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N6-(1-oxooctyl)-L-lysine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23735-96-8

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23735-96-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23735-96-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,7,3 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 23735-96:
(7*2)+(6*3)+(5*7)+(4*3)+(3*5)+(2*9)+(1*6)=118
118 % 10 = 8
So 23735-96-8 is a valid CAS Registry Number.
InChI:InChI=1/C14H28N2O3/c1-2-3-4-5-6-10-13(17)16-11-8-7-9-12(15)14(18)19/h12H,2-11,15H2,1H3,(H,16,17)(H,18,19)/t12-/m0/s1

23735-96-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N6-(1-oxooctyl)-L-lysine

1.2 Other means of identification

Product number -
Other names 2-Amino-6-octanoylamino-hexanoic acid

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:23735-96-8 SDS

23735-96-8Upstream product

23735-96-8Downstream Products

23735-96-8Relevant academic research and scientific papers

Acylation of amino acids

-

, (2008/06/13)

N-mono-substituted derivatives of diamino acids are prepared by the reaction of succinimidyl esters of carboxylic acids or substituted carbonic acids with the unprotected diamino acid. The acylation preferentially occurs at the side chain or terminal amino group of the diamino acid. For example, selective acylation of the terminal amino group of lysine occurs without first having protected the 2-amino group. Such acylation has application in the preparation of inter alia N6 -palmitoyl-lysine.

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