Cas 1196130-16-1,Nα-tert-butyloxycarbonyl-Nγ-(6-thiocyanatobenzothiazol-2-yl)asparagine benzyl ester

1196130-16-1

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Basic information

Product Name: Nα-tert-butyloxycarbonyl-Nγ-(6-thiocyanatobenzothiazol-2-yl)asparagine benzyl ester
Synonyms: Nα-tert-butyloxycarbonyl-Nγ-(6-thiocyanatobenzothiazol-2-yl)asparagine benzyl ester
CAS NO:1196130-16-1
Molecular Formula:
Molecular Weight: 512.61
EINECS: N/A
Product Categories: N/A
Mol File: 1196130-16-1.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: Nα-tert-butyloxycarbonyl-Nγ-(6-thiocyanatobenzothiazol-2-yl)asparagine benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Nα-tert-butyloxycarbonyl-Nγ-(6-thiocyanatobenzothiazol-2-yl)asparagine benzyl ester(1196130-16-1)
EPA Substance Registry System: Nα-tert-butyloxycarbonyl-Nγ-(6-thiocyanatobenzothiazol-2-yl)asparagine benzyl ester(1196130-16-1)

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: 1196130-16-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1196130-16-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,6,1,3 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1196130-16:
(9*1)+(8*1)+(7*9)+(6*6)+(5*1)+(4*3)+(3*0)+(2*1)+(1*6)=141
141 % 10 = 1
So 1196130-16-1 is a valid CAS Registry Number.

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1196130-16-1Relevant articles and documents

Unnatural benz-X-azolyl asparagine derivatives as novel fluorescent amino acids: synthesis and photophysical characterization

Esteves, Cátia I.C.,Silva, Ana M.F.,Raposo, M. Manuela M.,Costa, Susana P.G.

experimental part, p. 9373 - 9377 (2009/12/28)

A family of new asparagine derivatives bearing benzothiazole and benzimidazole units, functionalised with electron donor or acceptor groups, were synthesized in good to excellent yields. The photophysical characterization of these new heterocyclic amino a

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