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289471-18-7

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289471-18-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 289471-18-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,9,4,7 and 1 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 289471-18:
(8*2)+(7*8)+(6*9)+(5*4)+(4*7)+(3*1)+(2*1)+(1*8)=187
187 % 10 = 7
So 289471-18-7 is a valid CAS Registry Number.

289471-18-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl (4-benzoylphenyl)carbamate

1.2 Other means of identification

Product number -
Other names ethyl 4-benzoylphenylcarbamate

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:289471-18-7 SDS

289471-18-7Relevant articles and documents

Installation of protected ammonia equivalents onto aromatic & heteroaromatic rings in water enabled by micellar catalysis

Isley, Nicholas A.,Dobarco, Sebastian,Lipshutz, Bruce H.

supporting information, p. 1480 - 1488 (2014/03/21)

A single set of conditions consisting of a palladium catalyst, a commercially available ligand, and a base, allow for several types of C-N bond constructions to be conducted in water with the aid of a commercially available "designer" surfactant (TPGS-750-M). Products containing a protected NH2 group in the form of a carbamate, sulfonamide, or urea can be fashioned starting with aryl or heteroaryl bromides, iodides, and in some cases, chlorides, as substrates. Reaction temperatures are in the range of room temperature to, at most, 50 °C, and result in essentially full conversion and good isolated yields.

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