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1,2-Cyclohexanediol,3-methyl-6-(1-methylethyl)-,(1S,2R,3R,6S)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

308355-91-1

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308355-91-1 Usage

Explanation

The compound consists of 10 carbon atoms, 20 hydrogen atoms, and 2 oxygen atoms.

Explanation

It contains two hydroxyl (OH) groups attached to a cyclohexane ring.

Explanation

The core structure of the compound is a six-membered carbon ring, which is common in many organic compounds.

Explanation

This notation describes the spatial arrangement of the atoms in the molecule, which is crucial for its reactivity and potential applications.

Explanation

The molecule has a methyl group (CH3) at the 3rd position and an isopropyl group (C3H7) at the 6th position of the cyclohexane ring.

Explanation

Due to its specific structure and reactivity, the compound may be used in the synthesis of more complex molecules, in the pharmaceutical industry, or as a starting material for other chemical compounds.

Explanation

The reactivity of the compound is influenced by its molecular structure, stereochemistry, and the presence of functional groups, such as the hydroxyl groups.

Explanation

Information about the compound's physical properties, such as melting point, boiling point, or solubility, is not available in the given material.

Explanation

Information about the compound's chemical properties, such as acidity, basicity, or stability, is not available in the given material.

Type of molecule

Diol

Cyclohexane ring

6-membered carbon ring

Stereochemistry

(1S,2R,3R,6S)

Substituents

3-methyl and 6-(1-methylethyl) groups

Potential applications

Organic synthesis, pharmaceuticals, precursor to complex compounds

Reactivity

Depends on specific characteristics

Physical properties

Not provided in the material

Chemical properties

Not provided in the material

Check Digit Verification of cas no

The CAS Registry Mumber 308355-91-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,8,3,5 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 308355-91:
(8*3)+(7*0)+(6*8)+(5*3)+(4*5)+(3*5)+(2*9)+(1*1)=141
141 % 10 = 1
So 308355-91-1 is a valid CAS Registry Number.

308355-91-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ((1S,2R,35,6R)-2-hydroxy-3-isopropyl-6-methyl-cyclohexanol)

1.2 Other means of identification

Product number -
Other names (1R)-1r-Methyl-4t-isopropyl-cyclohexandiol-(2c.3c)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:308355-91-1 SDS

308355-91-1Downstream Products

308355-91-1Relevant academic research and scientific papers

Methods and systems for evaluating and predicting the reactivity of monooxygenase enzymes

-

Page/Page column 46; 47, (2016/04/20)

Methods and systems for evaluating and predicting the reactivity of natural and engineered monooxygenase enzymes are provided. Methods are provided for acquiring a functional profile (fingerprint) of monooxygenases that encode information regarding the ac

P450 fingerprinting method for rapid discovery of terpene hydroxylating P450 catalysts with diversified regioselectivity

Zhang, Kaidong,El Damaty, Shady,Fasan, Rudi

supporting information; experimental part, p. 3242 - 3245 (2011/05/04)

Engineered P450 enzymes constitute attractive catalysts for the selective oxidation of unactivated C-H bonds in complex molecules. A current bottleneck in the use of P450 catalysis for chemical synthesis is the time and effort required to identify the P45

Insight into acid-mediated asymmetric spirocyclization in the presence of a chiral diol

Kiguchi,Tsurusaki,Yamada,Aso,Tanaka,Sakai,Suemune

, p. 1536 - 1540 (2007/10/03)

Asymmetric spirocyclization based on intramolecular conjugate addition using a combination of a Lewis acid and an optically active cyclohexane-1,2-diol has been studied in connection with 1) the effect of substituents on the cyclohexane-1,2-diol and 2) th

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