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88194-93-8

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88194-93-8 Usage

Class

Organic compounds

Subclass

Hydrazines

Functional Group

Hydrazine group (two NH2 groups attached to a carbonyl group)

Ester

Diethyl ester of 1,2-hydrazinedicarboxylic acid

Applications

a. Synthesis of pharmaceuticals
b. Synthesis of organic compounds

Properties

a. Antimicrobial
b. Antifungal

Potential Uses

a. Preservative in various products

Safety Precautions

a. Potential health hazards
b. Toxic effects
c. Careful handling
d. Proper safety measures required

Check Digit Verification of cas no

The CAS Registry Mumber 88194-93-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,1,9 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 88194-93:
(7*8)+(6*8)+(5*1)+(4*9)+(3*4)+(2*9)+(1*3)=178
178 % 10 = 8
So 88194-93-8 is a valid CAS Registry Number.

88194-93-8SDS

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 diethyl N-(3-benzylaminopropyl)hydrazodicarboxylate

1.2 Other means of identification

Product number -
Other names -

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:88194-93-8 SDS

88194-93-8Downstream Products

88194-93-8Relevant articles and documents

Preparation of Azetidines from 1,3-Aminopropanols

Sammes, Peter G.,Smith, Steven

, p. 2415 - 2420 (2007/10/02)

The preparation of 1,3-amino alcohols by the reduction of azetidin-2-ones with diborane is described.New methods for the cyclisation of the aminopropanols to the corresponding azetidines are reported; these methods centre on the use of a modified Mitsunobu reaction.

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