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88674-90-2

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88674-90-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88674-90-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,6,7 and 4 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 88674-90:
(7*8)+(6*8)+(5*6)+(4*7)+(3*4)+(2*9)+(1*0)=192
192 % 10 = 2
So 88674-90-2 is a valid CAS Registry Number.

88674-90-2SDS

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 ethyl N-[[(Z)-(6-oxocyclohexa-2,4-dien-1-ylidene)methyl]amino]carbamate

1.2 Other means of identification

Product number -
Other names salicylidene ethyl carbazate

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:88674-90-2 SDS

88674-90-2Downstream Products

88674-90-2Relevant articles and documents

Synthesis, Spectral, X-Ray Diffraction, DFT, and Nematicidal Activity of Mixed Ligand Complexes of Ethyl 2-(2-Hydroxybenzylidine)-Hydrazine Carboxylate and 1,10-Phenanthroline with Some Transition Metals

Zordok, Wael Abd-allah,Sadeek, Sadeek Atia,El-Farargy, Ahmed F.,Abd El-Lattif, Nossa S.

, p. 1478 - 1495 (2017)

In this work, mixed ligand complexes derived from ethyl 2-(2-hydroxybenzylidine)-hydrazine carboxylate (HL) and 1,10-phenanthroline (Phen) as ligands were synthesized and their structures elucidated by elemental analysis, infrared (IR), electronic,1

Synthesis of o-acylarylcarboxylic esters: A new replacement of phenolic hydroxyl by a carbonyl group

Katritzky,Kotali

, p. 6781 - 6784 (2007/10/02)

A wide variety of the title esters are prepared in good yields via a new two step replacement of phenolic hydroxyl by an ethoxycarbonyl group.

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