Cas 460326-94-7,(S,S,S)-N-(2-benzyloxycarbonyl-isothiazolidine-1,1-dioxide-3-carbonyl)-histidyl-prolinamide

460326-94-7

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Basic information

Product Name: (S,S,S)-N-(2-benzyloxycarbonyl-isothiazolidine-1,1-dioxide-3-carbonyl)-histidyl-prolinamide
Synonyms:
CAS NO:460326-94-7
Molecular Formula:
Molecular Weight: 532.577
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,S,S)-N-(2-benzyloxycarbonyl-isothiazolidine-1,1-dioxide-3-carbonyl)-histidyl-prolinamide(CAS DataBase Reference)
NIST Chemistry Reference: (S,S,S)-N-(2-benzyloxycarbonyl-isothiazolidine-1,1-dioxide-3-carbonyl)-histidyl-prolinamide(460326-94-7)
EPA Substance Registry System: (S,S,S)-N-(2-benzyloxycarbonyl-isothiazolidine-1,1-dioxide-3-carbonyl)-histidyl-prolinamide(460326-94-7)

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: 460326-94-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 460326-94-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,0,3,2 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 460326-94:
(8*4)+(7*6)+(6*0)+(5*3)+(4*2)+(3*6)+(2*9)+(1*4)=137
137 % 10 = 7
So 460326-94-7 is a valid CAS Registry Number.

460326-94-7Upstream product

147878-95-3 (S)-2-Benzyloxycarbonyl-isothiazolidine-1,1-dioxide-3-carboxylic acid

460326-94-7Downstream Products

460326-94-7Relevant academic research and scientific papers

Synthesis and biological evaluation of a novel pyroglutamyl-modified TRH analogue

Brunetti,Cacciatore,Di Stefano,Dupre,Giorgi,Luisi,Michelotto,Orlando,Pinnen,Recinella,Sozio,Spirito

, p. 479 - 486 (2002)

The TRH analogue 3, incorporating the (S)-isothiazolidine-1,1-dioxide-3-carboxylic acid (1) moiety in place of the native L-pyroglutamic acid (pGlu) residue, has been synthesized and fully characterized by 1H and 13C NMR. The effects

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