Cas 1402222-60-9,4-chloro-N'-((4,6-diphenylfuro[3,4-d]thiazol-2-yl)diazenyl)benzohydrazide

1402222-60-9

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Basic information

Product Name: 4-chloro-N'-((4,6-diphenylfuro[3,4-d]thiazol-2-yl)diazenyl)benzohydrazide
Synonyms: 4-chloro-N'-((4,6-diphenylfuro[3,4-d]thiazol-2-yl)diazenyl)benzohydrazide
CAS NO:1402222-60-9
Molecular Formula:
Molecular Weight: 445.929
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: 4-chloro-N'-((4,6-diphenylfuro[3,4-d]thiazol-2-yl)diazenyl)benzohydrazide(CAS DataBase Reference)
NIST Chemistry Reference: 4-chloro-N'-((4,6-diphenylfuro[3,4-d]thiazol-2-yl)diazenyl)benzohydrazide(1402222-60-9)
EPA Substance Registry System: 4-chloro-N'-((4,6-diphenylfuro[3,4-d]thiazol-2-yl)diazenyl)benzohydrazide(1402222-60-9)

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: 1402222-60-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1402222-60-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,2,2,2 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1402222-60:
(9*1)+(8*4)+(7*0)+(6*2)+(5*2)+(4*2)+(3*2)+(2*6)+(1*0)=89
89 % 10 = 9
So 1402222-60-9 is a valid CAS Registry Number.

1402222-60-9Upstream product

1402222-60-9Downstream Products

1402222-60-9Relevant academic research and scientific papers

Facile selective synthesis of new furo[3,4-d[-1,3-thiazoles

Aly, Ashraf A.,Hassan, Alaa A.,Al-Qalawi, Husam R.M.,Ishak, Esam A.

, p. 419 - 426 (2012)

In presence of triethylamine, the reaction of substituted 2-aroyl-hydrazinecarbothioamides with 1,4-Diphenyl-but-2-yne-1,4-dione afforded novel furo[3,4-d]-1,3-thiazoles in good yield. The reaction mechanism suggests that the second molecule of 1,4-Diphen

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