Cas 910808-85-4,(R,R)-7'-iodo-N-carbobenzyloxytryptophyl-3',5'-dichloro-4'-methoxyphenylglycine tert-butyl ester

910808-85-4

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Basic information

Product Name: (R,R)-7'-iodo-N-carbobenzyloxytryptophyl-3',5'-dichloro-4'-methoxyphenylglycine tert-butyl ester
Synonyms: (R,R)-7'-iodo-N-carbobenzyloxytryptophyl-3',5'-dichloro-4'-methoxyphenylglycine tert-butyl ester
CAS NO:910808-85-4
Molecular Formula:
Molecular Weight: 752.433
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,R)-7'-iodo-N-carbobenzyloxytryptophyl-3',5'-dichloro-4'-methoxyphenylglycine tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (R,R)-7'-iodo-N-carbobenzyloxytryptophyl-3',5'-dichloro-4'-methoxyphenylglycine tert-butyl ester(910808-85-4)
EPA Substance Registry System: (R,R)-7'-iodo-N-carbobenzyloxytryptophyl-3',5'-dichloro-4'-methoxyphenylglycine tert-butyl ester(910808-85-4)

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: 910808-85-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 910808-85-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,0,8,0 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 910808-85:
(8*9)+(7*1)+(6*0)+(5*8)+(4*0)+(3*8)+(2*8)+(1*5)=164
164 % 10 = 4
So 910808-85-4 is a valid CAS Registry Number.

910808-85-4Upstream product

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910808-85-4Relevant academic research and scientific papers

Preparation of 7-halo-indoles by thallation of N-formylindoline and their attempted use for synthesis of the right-hand segment of chloropeptin

Yamada, Yaeko,Arima, Shiho,Okada, Chiharu,Akiba, Ai,Kai, Toshitsugu,Harigaya, Yoshihiro

, p. 788 - 794 (2006)

7-Substituted (Cl, Br, I) indoles were synthesized by using thallation of N-formylindoline as a key reaction. Two precursor tripeptides for the right-hand segment of chloropeptin were synthesized by using (R)-7′-iodo and 7′-bromotryptophans derived from each 7-substituted indole (I, Br) obtained by the above procedure.

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