Cas 1308652-45-0,2-{2-[N-(3,4-methylenedioxy)benzyl]carbamoyl}phenyl-2-[N-(4-methyl)phenyl]aminoacetic acid N-cyclohexyl amide

1308652-45-0

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Basic information

Product Name: 2-{2-[N-(3,4-methylenedioxy)benzyl]carbamoyl}phenyl-2-[N-(4-methyl)phenyl]aminoacetic acid N-cyclohexyl amide
Synonyms: 2-{2-[N-(3,4-methylenedioxy)benzyl]carbamoyl}phenyl-2-[N-(4-methyl)phenyl]aminoacetic acid N-cyclohexyl amide
CAS NO:1308652-45-0
Molecular Formula:
Molecular Weight: 499.61
EINECS: N/A
Product Categories: N/A
Mol File: 1308652-45-0.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: 2-{2-[N-(3,4-methylenedioxy)benzyl]carbamoyl}phenyl-2-[N-(4-methyl)phenyl]aminoacetic acid N-cyclohexyl amide(CAS DataBase Reference)
NIST Chemistry Reference: 2-{2-[N-(3,4-methylenedioxy)benzyl]carbamoyl}phenyl-2-[N-(4-methyl)phenyl]aminoacetic acid N-cyclohexyl amide(1308652-45-0)
EPA Substance Registry System: 2-{2-[N-(3,4-methylenedioxy)benzyl]carbamoyl}phenyl-2-[N-(4-methyl)phenyl]aminoacetic acid N-cyclohexyl amide(1308652-45-0)

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: 1308652-45-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1308652-45-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,8,6,5 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1308652-45:
(9*1)+(8*3)+(7*0)+(6*8)+(5*6)+(4*5)+(3*2)+(2*4)+(1*5)=150
150 % 10 = 0
So 1308652-45-0 is a valid CAS Registry Number.

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1308652-45-0Relevant articles and documents

Synthesis of diverse phenylglycine derivatives via transformation of Ugi four-component condensation primary adducts

Marcaccini, Stefano,Menchi, Gloria,Trabocchi, Andrea

experimental part, p. 2673 - 2675 (2011/06/10)

3-(N-Substituted)amino-4-arylamino-1H-isochromenones (isocoumarins) which can be regarded as the enediamine tautomers of the Ugi four-component condensation primary adducts between 2-formylbenzoic acids, arylamines, and isocyanides undergo a facile ring c

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