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81363-09-9

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81363-09-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81363-09-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,3,6 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 81363-09:
(7*8)+(6*1)+(5*3)+(4*6)+(3*3)+(2*0)+(1*9)=119
119 % 10 = 9
So 81363-09-9 is a valid CAS Registry Number.

81363-09-9SDS

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 α-chlorobenzyl chloroformate

1.2 Other means of identification

Product number -
Other names chlorocarbonic acid-(α-chloro-benzyl ester)

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:81363-09-9 SDS

81363-09-9Relevant articles and documents

N-(Pivaloyloxy)alkoxy-carbonyl Prodrugs of the Glutamine Antagonist 6-Diazo-5-oxo- l -norleucine (DON) as a Potential Treatment for HIV Associated Neurocognitive Disorders

Nedelcovych, Michael T.,Tenora, Luká?,Kim, Boe-Hyun,Kelschenbach, Jennifer,Chao, Wei,Hadas, Eran,Jan?a?ík, Andrej,Prchalová, Eva,Zimmermann, Sarah C.,Dash, Ranjeet P.,Gadiano, Alexandra J.,Garrett, Caroline,Furtmüller, Georg,Oh, Byoungchol,Brandacher, Gerald,Alt, Jesse,Majer, Pavel,Volsky, David J.,Rais, Rana,Slusher, Barbara S.

, p. 7136 - 7198 (2017)

Aberrant excitatory neurotransmission associated with overproduction of glutamate has been implicated in the development of HIV-associated neurocognitive disorders (HAND). The glutamine antagonist 6-diazo-5-oxo-l-norleucine (DON, 14) attenuates glutamate

Benzaldehyde-derived chloroformates and their application towards the synthesis of methoxyfenozide-N-[(acyloxy)benzyloxy]carbonyl derivatives

Mulvihill, Mark J,Nguyen, Duyan V.,MacDougall, Brian,Martinez-Teipel, Blanca,Joseph, Rhoda,Gallagher, James,Weaver, Damian,Gusev, Arkady,Chung, KiHo,Mathis, William

, p. 7751 - 7754 (2007/10/03)

The synthesis of a series of substituted benzaldehyde-derived chloroformates and their application towards the synthesis of a diverse series of novel insecticidally active carboxylic acid [N′-tert-butyl-N′-(3,5-dimethylbenzoyl)-N-(3-methoxy-2- methylbenzo

Process for the preparation of α-chlorinated chloroformates

-

, (2008/06/13)

Process for the preparation of α-chlorinated chloroformates with the formula STR1 where R is H, an aliphatic or aromatic hydrocarbon radical or heterocyclic radical, substituted or non-substituted and n an integer. The process consists of reacting ClCOOCCl3 or Cl3 COCOOCCl3 with an aldehyde with formula R--(CHO)n in the presence of a compound, which in the medium releases a pair of ions, the anion of which being a halide which can attack the aldehyde function, because of the weak attractive power of the cation of this compound.

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