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136656-76-3

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136656-76-3 Usage

General Description

(2S)-1-tert-butoxypropan-2-ol, also known as (S)-tert-butyl 3-hydroxy-2-methylpropanoate, is a chemical compound with the molecular formula C7H16O2. It is a chiral alcohol that is commonly used as a reagent in organic synthesis and as a solvent in various chemical reactions. (2S)-1-tert-butoxypropan-2-ol is a colorless liquid with a fruity odor and is soluble in water and most organic solvents. It is commonly used in the pharmaceutical industry, as well as in the production of fragrances and flavors. Additionally, it has applications in the production of polymers and as a stabilizer in the formulation of coatings and adhesives. Overall, (2S)-1-tert-butoxypropan-2-ol is a versatile and widely used compound with various industrial and commercial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 136656-76-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,6,5 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 136656-76:
(8*1)+(7*3)+(6*6)+(5*6)+(4*5)+(3*6)+(2*7)+(1*6)=153
153 % 10 = 3
So 136656-76-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H16O2/c1-6(8)5-9-7(2,3)4/h6,8H,5H2,1-4H3/t6-/m0/s1

136656-76-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-1-[(2-methylpropan-2-yl)oxy]propan-2-ol

1.2 Other means of identification

Product number -
Other names -

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:136656-76-3 SDS

136656-76-3Relevant articles and documents

A Facile Chemoenzymatic Route to Enantiomerically Pure Oxiranes: Building Blocks for Biologically Active Compounds

Goergens, Ulrich,Schneider, Manfred P.

, p. 1064 - 1066 (2007/10/02)

The enantiomerically pure building blocks (R)- and (S)-1-4 were prepared both by enantioselective, enzymatic hydrolysis and by acyl transfer, and subsequently converted into the corresponding enantiomerically pure oxiranes (R)-and (S)-7 and 8.

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