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36159-49-6

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36159-49-6 Usage

General Description

2-BUTYLCYCLOHEXANOL is a chemical compound with the molecular formula C10H20O, and it belongs to the family of alcohols. It is a colorless liquid with a pleasant odor, and it is commonly used as a fragrance ingredient in perfumes and personal care products. It is also used as a solvent in various industrial applications. 2-BUTYLCYCLOHEXANOL is known for its low toxicity and is considered to be relatively safe for use in consumer products. However, it should be handled with care and in accordance with safety guidelines to prevent any potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 36159-49-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,1,5 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 36159-49:
(7*3)+(6*6)+(5*1)+(4*5)+(3*9)+(2*4)+(1*9)=126
126 % 10 = 6
So 36159-49-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H20O/c1-2-3-6-9-7-4-5-8-10(9)11/h9-11H,2-8H2,1H3

36159-49-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-BUTYLCYCLOHEXANOL

1.2 Other means of identification

Product number -
Other names 2-N-BUTYL-1-CYCLOHEXANOL

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:36159-49-6 SDS

36159-49-6Downstream Products

36159-49-6Relevant articles and documents

Conformational effects on lipase-mediated acylations of 2-substituted cyclohexanols

Tanikaga, Rikuhei,Matsumoto, Yoshimasa,Sakaguchi, Maki,Koyama, Yohei,Ono, Kentaro

, p. 6781 - 6783 (2007/10/03)

Lipase-mediated acetylations of trans- and cis-2-substituted cyclohexanols gave the corresponding (1R)-cyclohexyl acetates and (1S)-cyclohexanols in high yields and ee, but c-4-tert-butyl-c-2-ethenyl-r-1-cyclohexanol was unreactive owing to the steric interaction between the axial OH group and the axial H atoms at the 3- and 5-positions. In the cis-isomer the OH group occupies an equatorial position to bind to the lipase, and less bulky axial alkenyl and alkynyl groups might not so much prevent acetylations than an alkyl group.

Structure and Reactivity of Novel Lithium Di-tert-butylphosphido(alkyl)cuprates

Martin, Stephen F.,Fishpaugh, Jeffrey R.,Power, John M.,Giolando, Dean M.,Jones, Richard A.,et al.

, p. 7226 - 7228 (2007/10/02)

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