Cas 609359-05-9,(R)-2-[(2S,3R)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-hydroxy-butyrylamino]-3-hydroxy-propionic acid methyl ester

609359-05-9

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Basic information

Product Name: (R)-2-[(2S,3R)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-hydroxy-butyrylamino]-3-hydroxy-propionic acid methyl ester
Synonyms: (R)-2-[(2S,3R)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-hydroxy-butyrylamino]-3-hydroxy-propionic acid methyl ester
CAS NO:609359-05-9
Molecular Formula:
Molecular Weight: 442.469
EINECS: N/A
Product Categories: N/A
Mol File: 609359-05-9.mol
Article Data: 2

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)-2-[(2S,3R)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-hydroxy-butyrylamino]-3-hydroxy-propionic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (R)-2-[(2S,3R)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-hydroxy-butyrylamino]-3-hydroxy-propionic acid methyl ester(609359-05-9)
EPA Substance Registry System: (R)-2-[(2S,3R)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-hydroxy-butyrylamino]-3-hydroxy-propionic acid methyl ester(609359-05-9)

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: 609359-05-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 609359-05-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,9,3,5 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 609359-05:
(8*6)+(7*0)+(6*9)+(5*3)+(4*5)+(3*9)+(2*0)+(1*5)=169
169 % 10 = 9
So 609359-05-9 is a valid CAS Registry Number.

609359-05-9Upstream product

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609359-05-9Relevant articles and documents

Synthetic studies on thiostrepton: Construction of thiostrepton analogues with the thiazoline-containing macrocycle

Nicolaou,Nevalainen, Marta,Zak, Mark,Bulat, Stephan,Bella, Marco,Safina, Brian S.

, p. 3418 - 3424 (2003)

Leading the way: The novel thiostrepton analogue 1 and its 5S, 6S diastereomer were synthesized through macrolactamization reactions. Forays towards the total synthesis of the natural product itself should follow a similar strategy.

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