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326479-99-6

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326479-99-6 Usage

Chemical Properties

White Solid

Check Digit Verification of cas no

The CAS Registry Mumber 326479-99-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,6,4,7 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 326479-99:
(8*3)+(7*2)+(6*6)+(5*4)+(4*7)+(3*9)+(2*9)+(1*9)=176
176 % 10 = 6
So 326479-99-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H17Cl2NO3/c1-9(2,3)15-8(14)12-6(4-10)7(13)5-11/h6-7,13H,4-5H2,1-3H3,(H,12,14)/t6-,7+/m0/s1

326479-99-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-[(2R,3S)-1,4-dichloro-3-hydroxybutan-2-yl]carbamate

1.2 Other means of identification

Product number -
Other names 2R-(t-Boc)amino-1,4-dichloro-3S-hydroxybutane

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:326479-99-6 SDS

326479-99-6Upstream product

326479-99-6Relevant articles and documents

Ethylaziridine derivatives and their preparation methods

-

, (2008/06/13)

This invention is related to new ethylaziridine derivatives of formula (I) and their preparation. The compounds are useful synthetic intermediates for the synthesis of HIV protease inhibitors and oligopeptide mimetics.

Synthesis of novel, optically active, heterocyclic amino alcohols through desymmetrization of a C2-symmetric cyclic sulfate

Kim, B. Moon,Bae, Sung Jin,Seomoon, Gunn

, p. 6921 - 6922 (2007/10/03)

A general and efficient method for the synthesis of optically active cis-4-amino-3-hydroxy-substituted heterocycles (1-4) has been developed through desymmetrization of a C2-symmetric cyclic sulfate chiron prepared from catalytic asymmetric dihydroxylation of 1,4-dichloro-trans-2-butene.

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