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Dodecanenitrile, 3-hydroxy-, (3R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

922527-71-7

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922527-71-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 922527-71-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,2,5,2 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 922527-71:
(8*9)+(7*2)+(6*2)+(5*5)+(4*2)+(3*7)+(2*7)+(1*1)=167
167 % 10 = 7
So 922527-71-7 is a valid CAS Registry Number.

922527-71-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (3R)-3-hydroxydodecanenitrile

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:922527-71-7 SDS

922527-71-7Relevant academic research and scientific papers

Studies towards lipid A: a synthetic strategy for the enantioselective preparation of 3-hydroxy fatty acids

Guaragna, Annalisa,Nisco, Mauro De,Pedatella, Silvana,Palumbo, Giovanni

, p. 2839 - 2841 (2006)

A short and efficient enantioselective synthesis of (R)-3-hydroxydodecanoic acid is described, involving a Sharpless asymmetric dihydroxylation to produce the required (R)-stereochemistry.

Total synthesis of fellutamides, lipopeptide proteasome inhibitors. More sustainable peptide bond formation

Pirrung, Michael C.,Zhang, Fa,Ambadi, Sudhakar,Gangadhara Rao

, p. 8367 - 8375 (2016/09/09)

Solution-phase syntheses of three bioactive natural products of mixed polypeptide-polyketide biogenesis, fellutamides A, B, and C, have been achieved. Three peptide bonds are generated without the use of coupling reagents in each synthesis of the fellutamides, which act against proteasomes.

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