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Quality products?make an important contribution to long-term revenue and profitability. Buy high quality and low price (1S-trans)-2-methyl-5-(1-methylvinyl)cyclohex-2-en-1-ol 2102-58-1 now
1.What is the (1S-trans)-2-methyl-5-(1-methylvinyl)cyclohex-2-en-1-ol ?
Used in Fragrance and Flavor Industry:
(1S-trans)-2-methyl-5-(1-methylvinyl)cyclohex-2-en-1-ol is utilized as a key ingredient in the creation of fragrances and flavors due to its distinctive aromatic properties. Its unique chemical structure contributes to the development of complex and appealing scents and tastes in various consumer products.
Used in Organic Synthesis:
(1S-trans)-2-methyl-5-(1-methylvinyl)cyclohex-2-en-1-ol serves as an intermediate in the synthesis of other organic compounds, playing a crucial role in the production of various chemical products. Its reactivity and structural features make it a versatile building block in organic chemistry for creating a wide array of molecules with different applications.
Used in Chemical Research:
(1S-trans)-2-methyl-5-(1-methylvinyl)cyclohex-2-en-1-ol is also employed in chemical research for studying reaction mechanisms, exploring new synthetic pathways, and developing innovative applications. Its unique properties allow researchers to investigate novel chemical transformations and understand the underlying principles of organic reactions.
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6485-40-1,2244-16-8
(R)-Carvone
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99-48-9,1197-06-4,1197-07-5,2102-58-1,2102-59-2,5157-78-8,5503-11-7,7632-16-8,18383-51-2,22567-18-6,20307-86-2
(4R,6R)-carveol
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18383-51-2,22567-18-6,20307-86-2
(-)-trans-carveol
| Conditions | Yield |
|---|---|
|
With
lithium aluminium tetrahydride;
In
diethyl ether;
at -78 ℃;
for 0.5h;
Title compound not separated from byproducts.;
|
94% |
|
With
lithium aluminium tetrahydride;
In
tetrahydrofuran;
at -15 ℃;
Yield given;
|
|
|
With
Al(OC3H7)3;
In
isopropyl alcohol;
|
|
|
With
sodium tetrahydroborate; amphiphilic carbohydrate;
In
water;
for 12h;
Yield given. Yields of byproduct given. Title compound not separated from byproducts;
Ambient temperature;
|
|
|
With
sodium tetrahydroborate; amphiphilic carbohydrate;
In
water;
for 12h;
Product distribution;
Ambient temperature;
stereoselectivity of redn.; other carbonyl compounds;
|
|
|
With
potassium hydroxide; hydrogen;
RuCl2<(R)-binap>(dmf)n*(R,R)-DPEN;
In
isopropyl alcohol;
at 28 ℃;
for 17h;
under 6080 Torr;
Product distribution;
var. of catalyst, diamine, pressure, time, asymmetric induction;
|
|
|
With
sodium tetrahydroborate; Sucrose;
In
water;
at 20 ℃;
for 12h;
|
|
|
With
allylic alcohol dehydrogenase from Nicotiana tabacum; NADPH; Triton X-100;
In
phosphate buffer;
at 35 ℃;
for 3h;
pH=7.4;
Enzyme kinetics;
|
|
|
With
sodium tetrahydroborate;
|
|
|
With
sodium tetrahydroborate; Sucrose;
In
water;
at 20 ℃;
for 12h;
|
|
|
With
4 A molecular sieve; 1-Indanol;
Zr(O-n-Pr)n-MCM-41;
In
n-heptane;
at 75 ℃;
for 5h;
Further Variations:;
Catalysts;
Reagents;
Product distribution;
Kinetics;
|
|
|
With
diisobutylaluminium hydride;
In
dichloromethane;
at -70 ℃;
for 1h;
|
|
|
With
dicarbonyl-(2,4-bis(trimethylsilyl)bicyclo[3.3.0]nona-1,4-dien-3-one)[acetonitrile]iron; isopropyl alcohol;
at 80 ℃;
for 18h;
optical yield given as %de;
diastereoselective reaction;
Inert atmosphere;
|
|
|
With
tropinone reductase of Cochlearia officinalis; NADPH;
In
methanol;
at 30 ℃;
for 1h;
pH=5;
Reagent/catalyst;
Kinetics;
|
|
|
With
diisobutylaluminium hydride;
In
tetrahydrofuran;
at -78 ℃;
Overall yield = 99 %;
Inert atmosphere;
|
66.667 % de |
|
With
glutamate dehydrogenase; D-glucose; LfSDR1 V186A, G92E, E141L varient; nicotinamide adenine dinucleotide phosphate;
In
aq. phosphate buffer; ethanol;
at 30 ℃;
for 12h;
pH=6;
Reagent/catalyst;
diastereoselective reaction;
Enzymatic reaction;
|
52 % de |
|
With
silver tetrafluoroborate; diphenylsilane; C33H43ClN3ORh;
In
dichloromethane;
at 40 ℃;
for 24h;
Overall yield = 97 percent; diastereoselective reaction;
Glovebox;
Sealed tube;
|
57.895 % de |
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2244-16-8,6485-40-1
(S)-p-mentha-6,8-dien-2-one
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99-48-9,1197-06-4,1197-07-5,2102-58-1,2102-59-2,5157-78-8,5503-11-7,7632-16-8,18383-51-2,22567-18-6,20307-86-2
(4R,6R)-carveol
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-
18383-51-2,22567-18-6,20307-86-2
(-)-trans-carveol
| Conditions | Yield |
|---|---|
|
With
hydrido(phosphonite)cobalt(I); 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane;
In
benzene;
at 20 ℃;
for 16h;
stereoselective reaction;
Sealed tube;
Inert atmosphere;
Darkness;
Schlenk technique;
|
74 % de |
2.What is the CAS number for (1S-trans)-2-methyl-5-(1-methylvinyl)cyclohex-2-en-1-ol ?
The CAS number of (1S-trans)-2-methyl-5-(1-methylvinyl)cyclohex-2-en-1-ol is 2102-58-1.
More information of (1S-trans)-2-methyl-5-(1-methylvinyl)cyclohex-2-en-1-ol 2102-58-1 are:
|
CAS?Number |
2102-58-1 |
|
Density |
0.949g/cm3 |
|
Boiling Point |
231.5°Cat760mmHg |
|
Flash Point |
91.2°C |
|
Vapor Pressure |
0.0117mmHg at 25°C |
|
Refractive Index |
1.497 |
|
HS CODE |
2906199090 |
|
PSA |
20.23000 |
|
LogP |
2.27970 |
|
Pka |
14.60±0.60(Predicted) |
3.What are another words for (1S-trans)-2-methyl-5-(1-methylvinyl)cyclohex-2-en-1-ol ?
Synonyms?for?(1S-trans)-2-methyl-5-(1-methylvinyl)cyclohex-2-en-1-ol 2102-58-1:2-Cyclohexen-1-ol,2-methyl-5-(1-methylethenyl)-, (1S-trans)-; p-Mentha-6,8-dien-2-ol,(2S,4R)-(-)- (8CI); (-)-(4R,6S)-Carveol; (-)-trans-Carveol; Carveol,trans-(-)-; l-trans-Carveol; trans-(-)-Carveol
4.What is the molecular formula of (1S-trans)-2-methyl-5-(1-methylvinyl)cyclohex-2-en-1-ol?
The chemical formula of ?(1S-trans)-2-methyl-5-(1-methylvinyl)cyclohex-2-en-1-ol is?C10H16 O which containing 10 Carbon atoms,16 Hydrogen atoms and 1 Oxygen atoms,and the molecular weight of??(1S-trans)-2-methyl-5-(1-methylvinyl)cyclohex-2-en-1-ol?is 152.236.
5.What is (1S-trans)-2-methyl-5-(1-methylvinyl)cyclohex-2-en-1-ol (2102-58-1) used for?
(1S-trans)-2-methyl-5-(1-methylvinyl)cyclohex-2-en-1-ol, a cyclohexenol type of cycloalkenol, is a colorless liquid chemical compound with the molecular formula C10H16O and a molecular weight of 152.23 g/mol. Its unique structure, featuring a methyl and a vinyl group, endows it with distinctive chemical properties, making it valuable for a range of industrial applications.
InChI:InChI=1/C10H16O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9-11H,1,5-6H2,2-3H3/t9-,10+/m1/s1
Relevant articles related to (1S-trans)-2-methyl-5-(1-methylvinyl)cyclohex-2-en-1-ol:
|
Article |
Source |
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Chiral Imidazo[1,5- a]pyridine-Oxazolines: A Versatile Family of NHC Ligands for the Highly Enantioselective Hydrosilylation of Ketones |
Chinna Ayya Swamy,Varenikov, Andrii,Ruiter, Graham De supporting information, p. 247 - 257 (2020/02/04) |
|
Artificial Light-Harvesting Complexes Enable Rieske Oxygenase Catalyzed Hydroxylations in Non-Photosynthetic cells |
Bloh, Jonathan Z.,Burek, Bastien O.,Feyza ?zgen, F.,Kourist, Robert,Runda, Michael E.,Schmidt, Sandy,Wied, Peter , p. 3982 - 3987 (2020/02/04) |
6.Buy (1S-trans)-2-methyl-5-(1-methylvinyl)cyclohex-2-en-1-ol with the best price .
Tianjin Boron PharmaTech Co.,Ltd. is a quality supplier of (1S-trans)-2-methyl-5-(1-methylvinyl)cyclohex-2-en-1-ol. Our main goal is customer satisfaction. Contact us to negotiate the best price for your business on (1S-trans)-2-methyl-5-(1-methylvinyl)cyclohex-2-en-1-ol 2102-58-1.
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