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Undecanamide,11-bromo-N-(phenylmethyl)-
Cas No: 71322-53-7
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Undecanamide,11-bromo-N-(phenylmethyl)-
Cas No: 71322-53-7
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Antimex Chemical Limied
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Undecanamide,11-bromo-N-(phenylmethyl)-
Cas No: 71322-53-7
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Hubei Jiutian Bio-medical Technology Co., Ltd
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71322-53-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71322-53-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,3,2 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 71322-53:
(7*7)+(6*1)+(5*3)+(4*2)+(3*2)+(2*5)+(1*3)=97
97 % 10 = 7
So 71322-53-7 is a valid CAS Registry Number.

InChI:InChI=1/C18H28BrNO/c19-15-11-6-4-2-1-3-5-10-14-18(21)20-16-17-12-8-7-9-13-17/h7-9,12-13H,1-6,10-11,14-16H2,(H,20,21)

71322-53-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name	N-benzyl-11-bromoundecanamide

1.2 Other means of identification

Product number	-
Other names	EINECS 275-330-3

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:71322-53-7 SDS

71322-53-7Upstream product

100-46-9 benzylamine

71322-53-7Downstream Products

71322-53-7Relevant articles and documents

TEMPO-Catalyzed Oxidative Amidation of Alcohols via Hexafluoroisopropyl Esters

Vatèle, Jean-Michel

, p. 2280 - 2284 (2015)

Stepwise oxidative amidation of alcohols using trichloroisocyanuric acid, a catalytic amount of TEMPO in combination with pyridine and hexafluoroisopropyl (HFIP) alcohol followed by amines is described. This procedure used HFIP esters as activating esters which were found to be very efficient acylating agents for amide bond formation. This process is compatible with a number of functional groups and acid-sensitive protecting groups.

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CAS

71322-53-7