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51335-83-2

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51335-83-2 Usage

Physical state

Colorless, viscous liquid

Odor

Faint

Common uses

a. Solvent
b. Intermediate in chemical and pharmaceutical production

Additional functions

a. Corrosion inhibitor for metals
b. Stabilizer and plasticizer for polymers

Potential applications

a. Medicine (due to antimicrobial properties)
b. Cosmetics (due to antioxidant properties)

Safety precautions

Handle with care and follow proper safety measures

Check Digit Verification of cas no

The CAS Registry Mumber 51335-83-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,3,3 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 51335-83:
(7*5)+(6*1)+(5*3)+(4*3)+(3*5)+(2*8)+(1*3)=102
102 % 10 = 2
So 51335-83-2 is a valid CAS Registry Number.

51335-83-2SDS

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 5,5-dimethylcyclohexane-1,3-diol

1.2 Other means of identification

Product number -
Other names cis-5.5-Dimethylcyclohexan-1,3-diol

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:51335-83-2 SDS

51335-83-2Relevant articles and documents

Acylative desymmetrization of cyclic meso-1,3-diols by chiral DMAP derivatives

Mandai, Hiroki,Hironaka, Tsubasa,Mitsudo, Koichi,Suga, Seiji

supporting information, p. 471 - 474 (2021/03/15)

An efficient enantioselective acylative desymmetrization of cyclic meso-1,3-diols was developed by using a chiral DMAP derivative 1e having a 1,1¤-binaphthyl unit. The reactions required only 0.5mol% of the catalyst and showed good to excellent enantioselectivity. With this transformation, 5a, a key building block for the synthesis of natural products, was easily obtained in almost enantiomerically pure form after a single recrystallization. Control experiments revealed that tert-alcohol units on the catalyst were responsible for both the catalytic activity and enantioselectivity.

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