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215322-65-9

215322-65-9

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215322-65-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 215322-65-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,3,2 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 215322-65:
(8*2)+(7*1)+(6*5)+(5*3)+(4*2)+(3*2)+(2*6)+(1*5)=99
99 % 10 = 9
So 215322-65-9 is a valid CAS Registry Number.

215322-65-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-allyl-2-(3-phenylprop-2-ynyl)malonic acid dimethyl ester

1.2 Other means of identification

Product number -
Other names 1,3-dimethyl 2-allyl-2-(3-phenylprop-2-yn-1-yl)malonate

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:215322-65-9 SDS

215322-65-9Relevant articles and documents

Atom-Economical Ni-Catalyzed Diborylative Cyclization of Enynes: Preparation of Unsymmetrical Diboronates

Cabrera-Lobera, Natalia,Quirós, M. Teresa,Brennessel, William W.,Neidig, Michael L.,Bu?uel, Elena,Cárdenas, Diego J.

supporting information, p. 6552 - 6556 (2019/08/20)

We report a Ni-catalyzed diborylative cyclization of enynes that affords carbo- and heterocycles containing both alkyl- and alkenylboronates. The reaction is fully atom-economical, shows a broad scope, and employs a powerful and inexpensive catalytic Ni-b

The role of cyclobutenes in gold(I)-catalysed skeletal rearrangement of 1,6-enynes

Escribano-Cuesta, Ana,Perez-Galan, Patricia,Herrero-Gomez, Elena,Sekine, Masaki,Braga, Ataualpa A. C.,Maseras, Feliu,Echavarren, Antonio M.

supporting information; experimental part, p. 6105 - 6111 (2012/09/05)

1,6-Enynes with electron-donating substituents at the alkyne undergo gold(i)-catalysed single cleavage skeletal rearrangement, whereas substrates with electron-withdrawing substituents evolve selectively to double cleavage rearrangement. Theoretical calcu

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