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62183-17-9

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62183-17-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62183-17-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,1,8 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 62183-17:
(7*6)+(6*2)+(5*1)+(4*8)+(3*3)+(2*1)+(1*7)=109
109 % 10 = 9
So 62183-17-9 is a valid CAS Registry Number.

62183-17-9SDS

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 methyl 3-benzamidoprop-2-enoate

1.2 Other means of identification

Product number -
Other names 3-BENZOYLAMINO 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:62183-17-9 SDS

62183-17-9Relevant articles and documents

Magnetically recyclable palladium nanoparticles (Fe3O4-Pd) for oxidative coupling between amides and olefins at room temperature

Pal, Chandan Kumar,Sahu, Swagatika,Sahu, Ranjan Kumar,Singh, Rajesh Kumar,Jena, Ashis Kumar

, (2019/06/21)

A convenient method for the synthesis of magnetically recyclable palladium nanoparticles (Fe3O4-Pd) is described. The catalytic application of the Fe3O4-Pd nanoparticles was explored for the first time in oxidat

A rapid access to substituted oxazoles via PIFA-mediated oxidative cyclization of enamides

Kamiya, Midori,Sonoda, Motohiro,Tanimori, Shinji

, p. 1247 - 1254 (2017/02/10)

A facile and rapid access to multi-substituted oxazoles has been achieved under mild reaction conditions in a short reaction time. Reaction of enamides 1 with [bis(trifluoroacetoxy)iodo]benzene (PIFA) in trifluoroethanol (TFE) at room temperature for 15?min afforded the desired oxazoles 2 in moderate to excellent yields (58–98%). A wide range of functional group tolerance has been observed for these transformations.

An electrochemical synthesis of 2-acetoxy-2-amino acid and 3-acetoxy-3-amino acid derivatives.

Iwasaki,Horikawa,Matsumoto,Miyoshi

, p. 2419 - 2423 (2007/10/06)

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