Cas 731002-68-9,2-<i>tert</i>-butoxycarbonylamino-4-[4-(<i>tert</i>-butoxycarbonylmethyl-carbamoyl)-benzylsulfanyl]-butyric acid methyl ester

731002-68-9

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Basic information

Product Name: 2-tert-butoxycarbonylamino-4-[4-(tert-butoxycarbonylmethyl-carbamoyl)-benzylsulfanyl]-butyric acid methyl ester
Synonyms: 2-tert-butoxycarbonylamino-4-[4-(tert-butoxycarbonylmethyl-carbamoyl)-benzylsulfanyl]-butyric acid methyl ester
CAS NO:731002-68-9
Molecular Formula:
Molecular Weight: 496.625
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: 2-tert-butoxycarbonylamino-4-[4-(tert-butoxycarbonylmethyl-carbamoyl)-benzylsulfanyl]-butyric acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-tert-butoxycarbonylamino-4-[4-(tert-butoxycarbonylmethyl-carbamoyl)-benzylsulfanyl]-butyric acid methyl ester(731002-68-9)
EPA Substance Registry System: 2-tert-butoxycarbonylamino-4-[4-(tert-butoxycarbonylmethyl-carbamoyl)-benzylsulfanyl]-butyric acid methyl ester(731002-68-9)

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: 731002-68-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 731002-68-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,1,0,0 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 731002-68:
(8*7)+(7*3)+(6*1)+(5*0)+(4*0)+(3*2)+(2*6)+(1*8)=109
109 % 10 = 9
So 731002-68-9 is a valid CAS Registry Number.

731002-68-9Upstream product

731002-68-9Downstream Products

731002-69-0 2-tert-butoxycarbonylamino-4-[4-(tert-butoxycarbonylmethyl-carbamoyl)-phenylmethanesulfinyl]-butyric acid methyl ester

731002-68-9Relevant academic research and scientific papers

Synthesis of S-alkyl L-homocysteine analogues of glutathione and their kinetic studies with γ-glutamyl transpeptidase

Lherbet, Christian,Gravel, Christian,Keillor, Jeffrey W.

, p. 3451 - 3455 (2004)

A series of S-alkyl L-homocysteine analogues of glutathione was synthesized with varied oxidation state of the sulfur and tested for inhibition of rat kidney γ-glutamyl transpeptidase (GGT). The strong selectivity of the enzyme with respect to the sulfur oxidation state reveals important information for the development of powerful competitive inhibitors.

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