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113643-84-8

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113643-84-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113643-84-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,6,4 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 113643-84:
(8*1)+(7*1)+(6*3)+(5*6)+(4*4)+(3*3)+(2*8)+(1*4)=108
108 % 10 = 8
So 113643-84-8 is a valid CAS Registry Number.

113643-84-8SDS

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 N-benzoyl-N1-(furoyl-2)hydrazine

1.2 Other means of identification

Product number -
Other names N'-benzoylfuran-2-carbohydrazide

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:113643-84-8 SDS

113643-84-8Relevant articles and documents

Facile synthesis and stracture of novel 2,5-disubstituted 1,3,4-selenadiazoles

Hua, Guoxiong,Li, Yang,Fuller, Amy L.,Slawin, Alexandra M.Z.,Woollins, J. Derek

experimental part, p. 1612 - 1618 (2009/08/09)

The reaction of hydrazide with carbony] chloride in the presence of sodium carbonates leads to the corresponding 1,2- diacylhydrazines [1a-t, R 1C(O)NHNHC(O)R2, R1 = aryl, R2 = aryl or alkyl] in moderate to excellent yield (57-90%). The latter reacts with 2,4-diphenyl-l,3-diselenadiphosphetane- 2,4-diselenide (Woollins' reagent, WR) in refluxing toluene to give a series of new 2,5-disubstituted 1,3,4-selenadiazoles (2a-t, 51-99% yield). All compounds were characterized spectroscopically and six compounds were characterized crystalloqraphically. Wiley-VCH Verlag GmbH & Co. KGaA.

Facile synthesis of symmetric and unsymmetric 1,3,4-oxadiazoles using 2-acyl(or aroyl)pyridazin-3-ones

Park, Yong-Dae,Kim, Jeum-Jong,Chung, Hyun-A,Kweon, Deok-Heon,Cho, Su-Dong,Lee, Sang-Gyeong,Yoon, Yong-Jin

, p. 560 - 564 (2007/10/03)

Symmetric and unsymmetric 1,3,4-oxadiazoles were synthesized in situ from hydrazine hydrate and the corresponding 2-acyl-4,5-dichloropyridazin-3-ones as acylating agents in polyphosphoric acid or BF3·OEt2 in excellent yields.

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