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2-Propenoic acid, 2-(bromomethyl)-3-(4-ethylphenyl)-, methyl ester, (2Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

213999-87-2

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213999-87-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 213999-87-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,3,9,9 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 213999-87:
(8*2)+(7*1)+(6*3)+(5*9)+(4*9)+(3*9)+(2*8)+(1*7)=172
172 % 10 = 2
So 213999-87-2 is a valid CAS Registry Number.

213999-87-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl (2Z)-2-(bromomethyl)-3-(4-ethylphenyl)prop-2-enoate

1.2 Other means of identification

Product number -
Other names (Z)-2-Bromomethyl-3-(4-ethyl-phenyl)-acrylic acid methyl 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:213999-87-2 SDS

213999-87-2Upstream product

213999-87-2Relevant academic research and scientific papers

Design, synthesis and evaluation of 3-arylidene azetidin-2-ones as potential antifungal agents against Alternaria solani Sorauer

Delong, Wang,Yongling, Wu,Lanying, Wang,Juntao, Feng,Xing, Zhang

, p. 6661 - 6673 (2017/11/17)

A new concise and facile method was explored to synthesize a collection of new 3-arylidene azetidin-2-ones, which could be regarded as the derivatives of the hybrid scaffold of bioactive natural cinnamamide and heterocycle azetidi-2-one. The structures of

Synthesis of thio-heterocyclic analogues from Baylis-Hillman bromides as potent cyclooxygenase-2 inhibitors

Santhoshi, Amlipur,Mahendar, Budde,Mattapally, Saidulu,Sadhu, Partha Sarathi,Banerjee, Sanjay Kumar,Jayathirtha Rao, Vaidya

supporting information, p. 1952 - 1957 (2014/04/17)

A series of thio-substituted pyrimidine, benzoxazole, benzothiazole and triazole analogues were synthesized from Baylis-Hillman bromides in a clean and efficient way. The synthesized twenty new compounds were subjected to in vitro COX-1 and COX-2 inhibito

Baylis-Hillman chemistry: A novel synthesis of functionalized 1,4-pentadienes

Basavaiah, Deevi,Kumaragurubaran, Nagaswamy,Sharada, Duddu S.

, p. 85 - 87 (2007/10/03)

A novel synthesis of functionalized 1,4-pentadienes via the reaction of acrylonitrile with allyl halides, derived from Baylis-Hillman adducts, in the presence of DABCO has been described, demonstrating for the first time the application of allyl halides a

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