Cas 1203948-45-1,(S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(2-tosylisoindolin-5-yl)propanoic acid,

1203948-45-1

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Basic information

Product Name: (S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(2-tosylisoindolin-5-yl)propanoic acid,
Synonyms: (S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(2-tosylisoindolin-5-yl)propanoic acid,
CAS NO:1203948-45-1
Molecular Formula:
Molecular Weight: 582.677
EINECS: N/A
Product Categories: N/A
Mol File: 1203948-45-1.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: (S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(2-tosylisoindolin-5-yl)propanoic acid,(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(2-tosylisoindolin-5-yl)propanoic acid,(1203948-45-1)
EPA Substance Registry System: (S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(2-tosylisoindolin-5-yl)propanoic acid,(1203948-45-1)

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: 1203948-45-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1203948-45-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,3,9,4 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1203948-45:
(9*1)+(8*2)+(7*0)+(6*3)+(5*9)+(4*4)+(3*8)+(2*4)+(1*5)=141
141 % 10 = 1
So 1203948-45-1 is a valid CAS Registry Number.

1203948-45-1Upstream product

1203948-45-1Downstream Products

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

1203948-45-1Relevant articles and documents

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

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

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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