Cas 173383-28-3,(R)-2-((R)-2-tert-Butoxycarbonylamino-4-methyl-pentanoylamino)-3-(3,5-dichloro-4-hydroxy-phenyl)-propionic acid

173383-28-3

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Basic information

Product Name: (R)-2-((R)-2-tert-Butoxycarbonylamino-4-methyl-pentanoylamino)-3-(3,5-dichloro-4-hydroxy-phenyl)-propionic acid
Synonyms:
CAS NO:173383-28-3
Molecular Formula:
Molecular Weight: 463.358
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)-2-((R)-2-tert-Butoxycarbonylamino-4-methyl-pentanoylamino)-3-(3,5-dichloro-4-hydroxy-phenyl)-propionic acid(CAS DataBase Reference)
NIST Chemistry Reference: (R)-2-((R)-2-tert-Butoxycarbonylamino-4-methyl-pentanoylamino)-3-(3,5-dichloro-4-hydroxy-phenyl)-propionic acid(173383-28-3)
EPA Substance Registry System: (R)-2-((R)-2-tert-Butoxycarbonylamino-4-methyl-pentanoylamino)-3-(3,5-dichloro-4-hydroxy-phenyl)-propionic acid(173383-28-3)

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: 173383-28-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 173383-28-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,3,8 and 3 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 173383-28:
(8*1)+(7*7)+(6*3)+(5*3)+(4*8)+(3*3)+(2*2)+(1*8)=143
143 % 10 = 3
So 173383-28-3 is a valid CAS Registry Number.

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173383-28-3Relevant academic research and scientific papers

Synthetic Studies on Vancomycin: Synthesis of Seco-Aglucovancomycins

Nakamura, Kazuhiko,Nishiyama, Shigeru,Yamamura, Shosuke

, p. 8621 - 8624 (1995)

Preparation of the vancomycin analogs (SAV-1 and SAV-2) is described.The key step is construction of a bicyclic diaryl ether residue by means of thallium(III) oxidation of the corresponding halogenated phenols.

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