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Benzeneethanehydrazonoyl bromide, a-oxo-N-(5-phenyl-1H-pyrazol-3-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

98664-16-5

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98664-16-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98664-16-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,6,6 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 98664-16:
(7*9)+(6*8)+(5*6)+(4*6)+(3*4)+(2*1)+(1*6)=185
185 % 10 = 5
So 98664-16-5 is a valid CAS Registry Number.

98664-16-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name C-benzoyl-N-(3-phenyl-5-pyrazolyl)formohydrazidoyl bromide

1.2 Other means of identification

Product number -
Other names α-bromo-α'(3-phenyl)pyrazolylglyoxalhydrazone

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:98664-16-5 SDS

98664-16-5Relevant academic research and scientific papers

Synthesis of Some New 2-Imino-2,3-dihydro-1,3,4-thiadiazole and Selenadiazole Derivatives

Abdelhamid, Abdou Osman,Shawali, A. S.

, p. 613 - 616 (2007/10/02)

Diazotized 3(5)-amino-5(3)-phenylpyrazole (2) reacts with phenacylthiocyanate (1) and phenacylselenocyanate (10) to give the corresponding 1,3,4-thiadiazoline derivative (5) and 1,3,4-selenadiazoline derivative (12), respectively.A mechanism is proposed and it is substantiated by an alternate synthesis of 5 and 12 from the corresponding hydrazidoyl bromide (6) with potassium thiocyanate and potassium selenocyanate, respectively.The thiadiazoline (5) and selenadiazoline (12) give the respective N-acyl derivatives (7a) and (12) with acetic anhydride.Nitrosation of 5 and 12 gives the corresponding N-nitroso-derivatives (8a) and (14), respectively.Cyclization of 6 gives the corresponding 9 with triethylamine in benzene. - 2-Imino-2,3-dihydro-1,3,4-thiadiazole, Selenadiazole Derivatives

The Structure of the Diazonium Coupling Products of Phenacyl Thiocyanate and Phenacyl Selenocyanate with Diazotized 3-Phenyl-5-Aminopyrazole

Farag, Ahmad M.,Fahmi, Abdelgawad A.,Abdelhamid, Abdou O.,Shawali, Ahmad S.,Algharib, Mohamed S.

, p. 1341 - 1344 (2007/10/02)

The reaction of diazotized 3-phenyl-5-aminopyrazole with phenacyl thiocyanate 1a and phenacyl selenocyanate 1b afforded directly 2-imino-3-(3-phenyl-5-pyrazolyl)-5-benzoyl-2,3-dihydro-1,3,4-thiadiazole monohydrate 9a and 2-imino-3-(3-phenyl-5-pyrazolyl)-5

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