Cas 37629-75-7,(Z)-3-(3,4-dichlorophenyl)-2-(3,4-dimethoxyphenyl)acrylonitrile

37629-75-7

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Basic information

Product Name: (Z)-3-(3,4-dichlorophenyl)-2-(3,4-dimethoxyphenyl)acrylonitrile
Synonyms: (Z)-3-(3,4-dichlorophenyl)-2-(3,4-dimethoxyphenyl)acrylonitrile
CAS NO:37629-75-7
Molecular Formula:
Molecular Weight: 334.202
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: (Z)-3-(3,4-dichlorophenyl)-2-(3,4-dimethoxyphenyl)acrylonitrile(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-3-(3,4-dichlorophenyl)-2-(3,4-dimethoxyphenyl)acrylonitrile(37629-75-7)
EPA Substance Registry System: (Z)-3-(3,4-dichlorophenyl)-2-(3,4-dimethoxyphenyl)acrylonitrile(37629-75-7)

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: 37629-75-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 37629-75-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,6,2 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 37629-75:
(7*3)+(6*7)+(5*6)+(4*2)+(3*9)+(2*7)+(1*5)=147
147 % 10 = 7
So 37629-75-7 is a valid CAS Registry Number.

37629-75-7Upstream product

37629-75-7Downstream Products

1619942-63-0 5-(3,4-dichlorophenyl)-4-(3,4-dimethoxyphenyl)-2H-1,2,3-triazole

37629-75-7Relevant academic research and scientific papers

Synthesis and biological evaluation of novel 4,5-disubstituted 2H-1,2,3-triazoles as cis-constrained analogues of combretastatin A-4

Madadi, Nikhil R.,Penthala, Narsimha R.,Howk, Kevin,Ketkar, Amit,Eoff, Robert L.,Borrelli, Michael J.,Crooks, Peter A.

, p. 123 - 132 (2015/09/15)

A series of combretastatin A-4 (CA-4) analogues have been prepared from (Z)-substituted diarylacrylonitriles (1a-1p) obtained in a two-step synthesis from appropriate arylaldehydes and acrylonitriles. The resulting 4,5-disubstituted 2H-1,2,3-triazoles wer

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