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76-35-7

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76-35-7 Usage

General Description

2,2-Dimethyl-1,3-butanediol is a chemical compound with the molecular formula C6H14O2. It is a colorless, odorless liquid that is commonly used as a solvent and a synthetic intermediate in the production of various other chemicals. It is also used as a potential alternative to traditional fossil fuels due to its renewable and sustainable nature. Additionally, 2,2-Dimethyl-1,3-butanediol has antimicrobial properties and is used in certain personal care products and pharmaceuticals. It is considered to be relatively low in toxicity and is generally regarded as safe for use in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 76-35-7 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 7 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 76-35:
(4*7)+(3*6)+(2*3)+(1*5)=57
57 % 10 = 7
So 76-35-7 is a valid CAS Registry Number.

76-35-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-dimethylbutane-1,3-diol

1.2 Other means of identification

Product number -
Other names 2,2-Dimethyl-1,3-butanediol

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:76-35-7 SDS

76-35-7Relevant articles and documents

Methylation-ring opening of 3,3-disubstituted 2,3-epoxy alcohols. Synthesis of chiral quaternary fragments for assembly of briaran diterpenes

Balasubramaniam, Rajiv P.,Moss, David K.,Wyatt, Justin K.,Spence, John D.,Gee, Arvin,Nantz, Michael H.

, p. 7429 - 7444 (2007/10/03)

Two chiral quaternary carbon-containing fragments suitable for elaboration to the briaran diterpenes were obtained by regioselective methylation of functionalized 3,3-disubstituted 2,3-epoxy-1-ols. The factors which favor methylation at the more hindered position of a trisubstituted 2,3-epoxy alcohol were determined.

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