Cas 670221-33-7,Acetic acid, [4-(3-chlorobenzoyl)-2-methylphenoxy]-, 2-[[(4-methylphenyl)amino]thioxomethyl]hydrazide

670221-33-7

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Basic information

Product Name: Acetic acid, [4-(3-chlorobenzoyl)-2-methylphenoxy]-, 2-[[(4-methylphenyl)amino]thioxomethyl]hydrazide
Synonyms:
CAS NO:670221-33-7
Molecular Formula: C24H22ClN3O3S
Molecular Weight: 467.976
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Acetic acid, [4-(3-chlorobenzoyl)-2-methylphenoxy]-, 2-[[(4-methylphenyl)amino]thioxomethyl]hydrazide(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid, [4-(3-chlorobenzoyl)-2-methylphenoxy]-, 2-[[(4-methylphenyl)amino]thioxomethyl]hydrazide(670221-33-7)
EPA Substance Registry System: Acetic acid, [4-(3-chlorobenzoyl)-2-methylphenoxy]-, 2-[[(4-methylphenyl)amino]thioxomethyl]hydrazide(670221-33-7)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 670221-33-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 670221-33-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,0,2,2 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 670221-33:
(8*6)+(7*7)+(6*0)+(5*2)+(4*2)+(3*1)+(2*3)+(1*3)=127
127 % 10 = 7
So 670221-33-7 is a valid CAS Registry Number.

670221-33-7Upstream product

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670221-33-7Relevant academic research and scientific papers

Synthesis and antimicrobial activity of 5-[(4-aroyl) aryloxymethyl]-2-(4-methylphenylamino)-1,3,4-thiadiazoles and 5-[(4-aroyl) aryloxy methyl]-4-(4-methylphenyl)-3-mercapto-4H-1,2,4-triazoles

Sudhab,Shashikanth,Khanum, Shaukath Ara

, p. 2652 - 2656 (2007/10/03)

Aroyl aryloxyacetic thiosemicarbazides 4a-d have been synthesized by the reaction of acid hydrazides 3a-d with p-tolyl isothiocyanate. The aroyl aryloxyacetic thiosemicarbazides 4a-d on intramolecular cyclization using conc.H2SO4 and

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