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55478-53-0

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55478-53-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55478-53-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,4,7 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 55478-53:
(7*5)+(6*5)+(5*4)+(4*7)+(3*8)+(2*5)+(1*3)=150
150 % 10 = 0
So 55478-53-0 is a valid CAS Registry Number.

55478-53-0SDS

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 5-oxopyrrolidine-2-carbonyl chloride

1.2 Other means of identification

Product number -
Other names 2-pyrrolidone-5-carbonyl chloride

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:55478-53-0 SDS

55478-53-0Relevant articles and documents

Calycosin derivative as well as preparation method and application thereof

-

Paragraph 0028; 0029' 0030, (2017/01/02)

The invention relates to a calycosin derivative as well as a preparation method and application thereof, belonging to the field of medicinal chemistry. The calycosin derivative is of a structure A shown in the specification, wherein R1 and R2 are out one

Haem d1: Development of a new coupling procedure leading to the synthesis of isobacteriochlorins

Mackman, Richard L.,Micklefield, Jason,Block, Michael H.,Leeper, Finian J.,Battersby, Alan R.

, p. 2111 - 2122 (2007/10/03)

A new approach has been developed for construction of the western and eastern lactams, e.g. 2 and 3, needed for synthesis of isobacteriochlorins. It involves acylation of pyrroles with lactonic acids to form ketones. These are then efficiently converted into the desired lactams by a short sequence of reactions. All the steps are high yielding and simple to carry out.

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