Cas 1415662-73-5,(2E)-3-(3,4-dimethoxyphenyl)-N-(6-nitro-1,3-benzothiazol-2-yl)acrylamide

1415662-73-5

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Basic information

Product Name: (2E)-3-(3,4-dimethoxyphenyl)-N-(6-nitro-1,3-benzothiazol-2-yl)acrylamide
Synonyms: (2E)-3-(3,4-dimethoxyphenyl)-N-(6-nitro-1,3-benzothiazol-2-yl)acrylamide
CAS NO:1415662-73-5
Molecular Formula:
Molecular Weight: 385.4
EINECS: N/A
Product Categories: N/A
Mol File: 1415662-73-5.mol
Article Data: 1

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: (2E)-3-(3,4-dimethoxyphenyl)-N-(6-nitro-1,3-benzothiazol-2-yl)acrylamide(CAS DataBase Reference)
NIST Chemistry Reference: (2E)-3-(3,4-dimethoxyphenyl)-N-(6-nitro-1,3-benzothiazol-2-yl)acrylamide(1415662-73-5)
EPA Substance Registry System: (2E)-3-(3,4-dimethoxyphenyl)-N-(6-nitro-1,3-benzothiazol-2-yl)acrylamide(1415662-73-5)

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: 1415662-73-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1415662-73-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,5,6,6 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1415662-73:
(9*1)+(8*4)+(7*1)+(6*5)+(5*6)+(4*6)+(3*2)+(2*7)+(1*3)=155
155 % 10 = 5
So 1415662-73-5 is a valid CAS Registry Number.

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1415662-73-5Relevant articles and documents

Synthesis of novel cinnamoyl amides using a solvent-free microwave-assisted method

Pellon, Rolando F.,Docampo, Maite L.

, p. 537 - 552 (2013/01/15)

A novel series of potential biologically active new cinnamoyl amides were synthesized in good yield and short reaction times. We have studied the one-pot, solvent-free reaction of cinnamic acid derivatives with aromatic amines using 1,3-dicyclohexylcarbodiimide under microwave irradiation in the presence of small quantities of dimethylformamide to improve energy transfer.

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