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86031-24-5

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86031-24-5 Usage

Uses

O-[(1,1-Dimethylethoxy)carbonyl]hydroxylamine is used as a reactant in the PEGylation and dimerization of expressed proteins.

Check Digit Verification of cas no

The CAS Registry Mumber 86031-24-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,0,3 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 86031-24:
(7*8)+(6*6)+(5*0)+(4*3)+(3*1)+(2*2)+(1*4)=115
115 % 10 = 5
So 86031-24-5 is a valid CAS Registry Number.

86031-24-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name amino tert-butyl carbonate

1.2 Other means of identification

Product number -
Other names [(tert-butoxycarbonyl)oxonio]azanide

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:86031-24-5 SDS

86031-24-5Upstream product

86031-24-5Relevant articles and documents

SYNTHESIS OF tert-BUTYL AMINOCARBONATE, A NEW TYPE OF COMPOUND THAT CAN BE USED TO ACYLATE AMINES

Harris, Robert B.,Wilson, Irwin B.

, p. 231 - 232 (1983)

tert-Butyl aminocarbonate (tert-butyloxycarbonyloxyamine) was prepared by reaction of hydroxylamine with excess di-tert-butyl dicarbonate.Amino carbonates have not previously been described.This compound rapidly acylates amines in both organic and aqueous solutions.

Sodium channel drugs and uses

-

, (2008/06/13)

The compounds of this invention comprise 2-10 ligands covalently connected, each of the ligands being capable of binding to a ligand binding site in a Na+channel, thereby modulating the biological activities thereof.

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