Cas 477335-39-0,O-benzyl-N<sup>a</sup>-(9-fluorenylmethoxycarbonyl)-N<sup>im</sup>-(triphenylmethyl)-(S)-erythro-3-hydroxyhistidine

477335-39-0

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Basic information

Product Name: O-benzyl-N^a-(9-fluorenylmethoxycarbonyl)-N^im-(triphenylmethyl)-(S)-erythro-3-hydroxyhistidine
Synonyms: O-benzyl-N^a-(9-fluorenylmethoxycarbonyl)-N^im-(triphenylmethyl)-(S)-erythro-3-hydroxyhistidine
CAS NO:477335-39-0
Molecular Formula:
Molecular Weight: 725.844
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: O-benzyl-N^a-(9-fluorenylmethoxycarbonyl)-N^im-(triphenylmethyl)-(S)-erythro-3-hydroxyhistidine(CAS DataBase Reference)
NIST Chemistry Reference: O-benzyl-N^a-(9-fluorenylmethoxycarbonyl)-N^im-(triphenylmethyl)-(S)-erythro-3-hydroxyhistidine(477335-39-0)
EPA Substance Registry System: O-benzyl-N^a-(9-fluorenylmethoxycarbonyl)-N^im-(triphenylmethyl)-(S)-erythro-3-hydroxyhistidine(477335-39-0)

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: 477335-39-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 477335-39-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,7,3,3 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 477335-39:
(8*4)+(7*7)+(6*7)+(5*3)+(4*3)+(3*5)+(2*3)+(1*9)=180
180 % 10 = 0
So 477335-39-0 is a valid CAS Registry Number.

477335-39-0Upstream product

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477335-39-0Relevant academic research and scientific papers

Solid-phase synthesis of bleomycin A5 and three monosaccharide analogues: Exploring the role of the carbohydrate moiety in RNA cleavage

Thomas, Craig J.,Chizhov, Alexander O.,Leitheiser, Christopher J.,Rishel, Michael J.,Konishi, Kazuhide,Tao, Zhi-Fu,Hecht, Sidney M.

, p. 12926 - 12927 (2002)

The solid-phase synthesis of bleomycin A5 (BLM A5) and three monosaccharide analogues is presented. The monosaccharide analogues incorporated α-D-mannose, α-L-gulose, and α-L-rhamnose moieties in lieu of the disaccharide normally pre

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