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53602-19-0

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53602-19-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53602-19-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,0 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53602-19:
(7*5)+(6*3)+(5*6)+(4*0)+(3*2)+(2*1)+(1*9)=100
100 % 10 = 0
So 53602-19-0 is a valid CAS Registry Number.

53602-19-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl N-(3-chloropropyl)carbamate

1.2 Other means of identification

Product number -
Other names Carbamic acid,(3-chloropropyl)-,phenylmethyl 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:53602-19-0 SDS

53602-19-0Downstream Products

53602-19-0Relevant articles and documents

Solvent-free Synthesis and Properties of Functionalized Hydrazines and Bishydrazines as Energetic Ingredients for Propulsion Applications

Eymann, John,Dhenain, Anne,Joucla, Lionel,Jacob, Guy,Lac?te, Emmanuel,Darwich, Chaza

supporting information, p. 4347 - 4357 (2020/11/30)

Functionalized hydrazines and bishydrazines are interesting straightforward precursors for accessing higher nitrogenated compounds. They offer structural diversity and promising energetic properties as well, namely for propulsion applications. A novel and

Reaction of N-alkyl azetidines with triphosgene

Menguy, Laurence,Drouillat, Bruno,Couty, Fran?ois

, p. 6625 - 6628 (2015/11/09)

N-Alkyl azetidines react with triphosgene (BTC) following two possible pathways: N-alkyl ring scission or ring cleavage, to give cyclic or acyclic N-carbamoyl chlorides. Predominance of one pathway over the other is governed by the nature of the substituents on the azetidine ring and on the nitrogen atom as well as by the relative stereochemistry of the ring substituents, and is examined in detail. Some azetidines were identified for their privileged reaction pathway, leading to new functionalized building blocks that were further elaborated into five- or six-membered urea or into azetidinic urea.

PEPTIDYL DERIVATIVES AS METALLOPROTEINASE INHIBITORS

-

, (2008/06/13)

Peptidyl derivatives are disclosed that are orally active metalloproteinase inhibitors. The peptidyl derivatives have a selective gelatinase action, have a long duration of action, and are useful in the prophylaxis or treatment of diseases or disorders in which stromelysis, collagenase or gelatinase have a role, for example, in the treatment of cancer to control the development of tumor metastases.

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