Cas 403709-34-2,6,7-dideoxy-2-O-phenoxycarbonyl-5-O-[3,4,6-tri-O-acetyl-2-deoxy-2-(2,2,2-trichloroacetamido)-β-D-glucopyranosyl]-L-galacto-hept-6-enono-1,4-lactone

403709-34-2

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Basic information

Product Name: 6,7-dideoxy-2-O-phenoxycarbonyl-5-O-[3,4,6-tri-O-acetyl-2-deoxy-2-(2,2,2-trichloroacetamido)-β-D-glucopyranosyl]-L-galacto-hept-6-enono-1,4-lactone
Synonyms: 6,7-dideoxy-2-O-phenoxycarbonyl-5-O-[3,4,6-tri-O-acetyl-2-deoxy-2-(2,2,2-trichloroacetamido)-β-D-glucopyranosyl]-L-galacto-hept-6-enono-1,4-lactone
CAS NO:403709-34-2
Molecular Formula:
Molecular Weight: 726.903
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: 6,7-dideoxy-2-O-phenoxycarbonyl-5-O-[3,4,6-tri-O-acetyl-2-deoxy-2-(2,2,2-trichloroacetamido)-β-D-glucopyranosyl]-L-galacto-hept-6-enono-1,4-lactone(CAS DataBase Reference)
NIST Chemistry Reference: 6,7-dideoxy-2-O-phenoxycarbonyl-5-O-[3,4,6-tri-O-acetyl-2-deoxy-2-(2,2,2-trichloroacetamido)-β-D-glucopyranosyl]-L-galacto-hept-6-enono-1,4-lactone(403709-34-2)
EPA Substance Registry System: 6,7-dideoxy-2-O-phenoxycarbonyl-5-O-[3,4,6-tri-O-acetyl-2-deoxy-2-(2,2,2-trichloroacetamido)-β-D-glucopyranosyl]-L-galacto-hept-6-enono-1,4-lactone(403709-34-2)

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: 403709-34-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 403709-34-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,3,7,0 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 403709-34:
(8*4)+(7*0)+(6*3)+(5*7)+(4*0)+(3*9)+(2*3)+(1*4)=122
122 % 10 = 2
So 403709-34-2 is a valid CAS Registry Number.

403709-34-2Upstream product

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403709-34-2Relevant academic research and scientific papers

Synthesis of a building block for phosphonate analogues of moenomycin A12 from D-tartaric acid

Zahra, Jalal,Hennig, Lothar,Findeisen, Matthias,Giesa, Sabine,Welzel, Peter,Müller, Dietrich,Sheldrick, William S

, p. 9437 - 9452 (2007/10/03)

An approach for the synthesis of moenomycin A12 C-glycoside partial structures is reported based on allyltin chemistry.

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