Cas 1308652-48-3,2-[N-(3-chloro)phenyl]amino-2-{2-[N-(4-methylbenzyl)carbamoyl]phenyl}acetic acid N-cyclohexyl amide

1308652-48-3

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Basic information

Product Name: 2-[N-(3-chloro)phenyl]amino-2-{2-[N-(4-methylbenzyl)carbamoyl]phenyl}acetic acid N-cyclohexyl amide
Synonyms: 2-[N-(3-chloro)phenyl]amino-2-{2-[N-(4-methylbenzyl)carbamoyl]phenyl}acetic acid N-cyclohexyl amide
CAS NO:1308652-48-3
Molecular Formula:
Molecular Weight: 490.045
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: 2-[N-(3-chloro)phenyl]amino-2-{2-[N-(4-methylbenzyl)carbamoyl]phenyl}acetic acid N-cyclohexyl amide(CAS DataBase Reference)
NIST Chemistry Reference: 2-[N-(3-chloro)phenyl]amino-2-{2-[N-(4-methylbenzyl)carbamoyl]phenyl}acetic acid N-cyclohexyl amide(1308652-48-3)
EPA Substance Registry System: 2-[N-(3-chloro)phenyl]amino-2-{2-[N-(4-methylbenzyl)carbamoyl]phenyl}acetic acid N-cyclohexyl amide(1308652-48-3)

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: 1308652-48-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1308652-48-3 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 8 respectively.
Calculate Digit Verification of CAS Registry Number 1308652-48:
(9*1)+(8*3)+(7*0)+(6*8)+(5*6)+(4*5)+(3*2)+(2*4)+(1*8)=153
153 % 10 = 3
So 1308652-48-3 is a valid CAS Registry Number.

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1308652-48-3Relevant academic research and scientific papers

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

Marcaccini, Stefano,Menchi, Gloria,Trabocchi, Andrea

, p. 2673 - 2675 (2011)

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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