Cas 194663-63-3,Phthalic acid 1-((2S,3R,4S)-5-tert-butoxycarbonylamino-2,3,4-trimethoxy-pentyl) ester 2-pentachlorophenyl ester

194663-63-3

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Basic information

Product Name: Phthalic acid 1-((2S,3R,4S)-5-tert-butoxycarbonylamino-2,3,4-trimethoxy-pentyl) ester 2-pentachlorophenyl ester
Synonyms: Phthalic acid 1-((2S,3R,4S)-5-tert-butoxycarbonylamino-2,3,4-trimethoxy-pentyl) ester 2-pentachlorophenyl ester
CAS NO:194663-63-3
Molecular Formula:
Molecular Weight: 689.802
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: Phthalic acid 1-((2S,3R,4S)-5-tert-butoxycarbonylamino-2,3,4-trimethoxy-pentyl) ester 2-pentachlorophenyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Phthalic acid 1-((2S,3R,4S)-5-tert-butoxycarbonylamino-2,3,4-trimethoxy-pentyl) ester 2-pentachlorophenyl ester(194663-63-3)
EPA Substance Registry System: Phthalic acid 1-((2S,3R,4S)-5-tert-butoxycarbonylamino-2,3,4-trimethoxy-pentyl) ester 2-pentachlorophenyl ester(194663-63-3)

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: 194663-63-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 194663-63-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,6,6 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 194663-63:
(8*1)+(7*9)+(6*4)+(5*6)+(4*6)+(3*3)+(2*6)+(1*3)=173
173 % 10 = 3
So 194663-63-3 is a valid CAS Registry Number.

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194663-63-3Relevant academic research and scientific papers

Synthesis and condensation reactions of 1-amino-1-deoxy-2,3,4-tri- O-methyl-5-O-[(pentachlorophenoxy) phthaloyl]-L-arabinitol

Molina Pinilla, Inmaculada,Bueno Martinez, Manuel,Galbis, Juan A.

, p. 241 - 244 (1997)

1-Amino-1-deoxy-2,3,4-tri-O-methyl-5-O-[(pentachlorophenoxy)phthaloyl]-L -arabinitol hydrochloride was prepared from L-arabinose, and its inter- and intra-molecular condensation reactions were studied, In these reactions, a mixture of oligomers (in HMPA: 30%) besides the monomeric compound 2,3,4-tri-O-methyl-1-deoxy-1-phthalimido-L-arabinitol (in HMPA: 51%) were obtained.

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