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13949-99-0

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13949-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13949-99-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,4 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13949-99:
(7*1)+(6*3)+(5*9)+(4*4)+(3*9)+(2*9)+(1*9)=140
140 % 10 = 0
So 13949-99-0 is a valid CAS Registry Number.

13949-99-0SDS

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 trans,meso-cyclopropanetricarboxylic acid triethyl ester

1.2 Other means of identification

Product number -
Other names trans,meso-triethyl cyclopropane-1,2,3-tricarboxylate

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:13949-99-0 SDS

13949-99-0Relevant articles and documents

Enantiodivergent syntheses of (-)- and (+)-dysibetaine CPa and N-desmethyl analog

Sakai, Michihiro,Tanaka, Kento,Takamizawa, Satoshi,Oikawa, Masato

, p. 4587 - 4594 (2014)

The first total syntheses of (-)-dysibetaine CPa and the antipode have been achieved using enantioselective solvolysis of meso-cyclic anhydride mediated by quinine derivative as an organocatalyst. The synthesis features a demonstration of an enantiodiverg

Simple large-scale preparation of 1,2,3-tris-acceptor substituted cyclopropanes

Kozhushkov, Sergei I.,Leonov, Andrei,De Meijere, Armin

, p. 956 - 958 (2007/10/03)

Triethyl (1α,2α,3β)cyclopropane-1,2,3-tricarboxylate (3aa), as well as diethyl (4ab) and dimethyl (1α,2β,3α)-1-acetylcyclopropane-2,3-dicarboxylate (4bb) have been prepared on a scale of up to 60 g by Michael initiated ring-closure (MIRC) cyclopropanation of dialkyl fumarates 1a,b with ethyl chloroacetate (2a) and chloroacetone (2b) in 62%, 51% and 56% yield, respectively. For the success of the new procedure it is essential to slowly add (within 5-7 h) the mixture of compounds 1 and 2 to a vigorously stirred suspension of K2CO3 in DMF in the presence of benzyltriethylammonium chloride.

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