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87247-19-6

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87247-19-6 Usage

General Description

(2S)-6-Methylheptan-2-ol is a colorless liquid compound with a chemical formula of C8H18O. It is also known as 6-Methylheptan-2-ol and is classified as a secondary alcohol. (2S)-6-Methylheptan-2-ol is widely used in the fragrance and flavor industry due to its pleasant, fruity aroma. It is also used as a solvent or a chemical intermediate in the production of various other chemicals. Additionally, (2S)-6-Methylheptan-2-ol has been found to have antimicrobial and insecticidal properties, making it useful in certain agricultural and pharmaceutical applications. Overall, this chemical compound has a variety of uses and applications in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 87247-19-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,2,4 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 87247-19:
(7*8)+(6*7)+(5*2)+(4*4)+(3*7)+(2*1)+(1*9)=156
156 % 10 = 6
So 87247-19-6 is a valid CAS Registry Number.

87247-19-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-6-methylheptan-2-ol

1.2 Other means of identification

Product number -
Other names (S)-6-methylheptan-2-ol

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:87247-19-6 SDS

87247-19-6Downstream Products

87247-19-6Relevant articles and documents

-

Doering,Young

, (1952)

-

Fragrance compositions and compounds

-

, (2012/01/14)

A perfume composition including the compound 4-[(1,5-dimethylhexyl)oxy]butanal in both its racemic and enantiomeric forms.

Asymmetric reduction of ketones by Geotrichum candidum in the presence of Amberlite Xad, A solid organic solvent

Nakamura, Kaoru,Fujii, Mikio,Ida, Yoshiteru

, p. 3205 - 3211 (2007/10/03)

Asymmetric reduction of ketones by Geotrichum candidum in the presence of Amberlite XAD, a solid organic solvent, was described. A hydrophobic polymer, XAD, was used as material to control the stereochemical course of microbial reductions. Aliphatic and aromatic ketones were reduced to the corresponding (S)-alcohols in excellent enantiomeric excess (ee) in the presence of XRD while low enantioselectivities were observed in the absence of the polymer.

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