Cas 1264273-01-9,(S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(2-tosylisoindolin-5-yl)propanoic acid methyl ester

1264273-01-9

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Basic information

Product Name: (S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(2-tosylisoindolin-5-yl)propanoic acid methyl ester
Synonyms: (S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(2-tosylisoindolin-5-yl)propanoic acid methyl ester
CAS NO:1264273-01-9
Molecular Formula:
Molecular Weight: 596.704
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: (S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(2-tosylisoindolin-5-yl)propanoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(2-tosylisoindolin-5-yl)propanoic acid methyl ester(1264273-01-9)
EPA Substance Registry System: (S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(2-tosylisoindolin-5-yl)propanoic acid methyl ester(1264273-01-9)

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: 1264273-01-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1264273-01-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,4,2,7 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1264273-01:
(9*1)+(8*2)+(7*6)+(6*4)+(5*2)+(4*7)+(3*3)+(2*0)+(1*1)=139
139 % 10 = 9
So 1264273-01-9 is a valid CAS Registry Number.

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1264273-01-9Relevant academic research and scientific papers

Synthesis of non-proteinogenic phenylalanine derivatives by rhodium-catalyzed [2+2+2] cycloaddition reactions

Garcia, Lidia,Pla-Quintana, Anna,Roglans, Anna

supporting information; experimental part, p. 5020 - 5027 (2010/02/15)

Non-proteinogenic phenylalanine derivatives were efficiently prepared by Rh(I)-catalyzed [2+2+2] cycloaddition reactions between enantiopure and racemic propargylglycine amino acids, with different protective groups, and diynes. Diverse substituents, incl

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