Cas 152983-19-2,(R)-2-Benzyloxycarbonylamino-4-(2-tert-butoxycarbonylamino-ethylsulfamoyl)-butyric acid benzyl ester

152983-19-2

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Basic information

Product Name: (R)-2-Benzyloxycarbonylamino-4-(2-tert-butoxycarbonylamino-ethylsulfamoyl)-butyric acid benzyl ester
Synonyms: (R)-2-Benzyloxycarbonylamino-4-(2-tert-butoxycarbonylamino-ethylsulfamoyl)-butyric acid benzyl ester
CAS NO:152983-19-2
Molecular Formula:
Molecular Weight: 549.645
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: (R)-2-Benzyloxycarbonylamino-4-(2-tert-butoxycarbonylamino-ethylsulfamoyl)-butyric acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (R)-2-Benzyloxycarbonylamino-4-(2-tert-butoxycarbonylamino-ethylsulfamoyl)-butyric acid benzyl ester(152983-19-2)
EPA Substance Registry System: (R)-2-Benzyloxycarbonylamino-4-(2-tert-butoxycarbonylamino-ethylsulfamoyl)-butyric acid benzyl ester(152983-19-2)

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: 152983-19-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 152983-19-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,9,8 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 152983-19:
(8*1)+(7*5)+(6*2)+(5*9)+(4*8)+(3*3)+(2*1)+(1*9)=152
152 % 10 = 2
So 152983-19-2 is a valid CAS Registry Number.

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152983-19-2Relevant academic research and scientific papers

Tmob Side Chain-Protected S-Cysteine- and Homo-S-cysteinesulfonamides, their Nα-Protected and Nω-Aminoethylated Derivatives

Videnov, Georgi,Aleksiev, Boris,Stoev, Mincho,Paipanova, Tamara,Jung, Guenther

, p. 941 - 946 (2007/10/02)

The 2,4,6-trimethoxybenzyl (Tmob) group is very suitable for temporary protection of the aminosulfonyl group of S-cysteine- and homo-S-cysteinesulfonamides.Both the introduction and removal of the Tmob-protecting group can be achieved in high yields. 2-Am

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