Cas 502186-10-9,pentachlorophenyl 3,4,5,7-tetra-O-acetyl-2-bromo-2-deoxy-α-D-galacto-hept-2-ulopyranosonate

502186-10-9

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Basic information

Product Name: pentachlorophenyl 3,4,5,7-tetra-O-acetyl-2-bromo-2-deoxy-α-D-galacto-hept-2-ulopyranosonate
Synonyms: pentachlorophenyl 3,4,5,7-tetra-O-acetyl-2-bromo-2-deoxy-α-D-galacto-hept-2-ulopyranosonate
CAS NO:502186-10-9
Molecular Formula:
Molecular Weight: 703.536
EINECS: N/A
Product Categories: N/A
Mol File: 502186-10-9.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: pentachlorophenyl 3,4,5,7-tetra-O-acetyl-2-bromo-2-deoxy-α-D-galacto-hept-2-ulopyranosonate(CAS DataBase Reference)
NIST Chemistry Reference: pentachlorophenyl 3,4,5,7-tetra-O-acetyl-2-bromo-2-deoxy-α-D-galacto-hept-2-ulopyranosonate(502186-10-9)
EPA Substance Registry System: pentachlorophenyl 3,4,5,7-tetra-O-acetyl-2-bromo-2-deoxy-α-D-galacto-hept-2-ulopyranosonate(502186-10-9)

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: 502186-10-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 502186-10-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,2,1,8 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 502186-10:
(8*5)+(7*0)+(6*2)+(5*1)+(4*8)+(3*6)+(2*1)+(1*0)=109
109 % 10 = 9
So 502186-10-9 is a valid CAS Registry Number.

502186-10-9Upstream product

502186-10-9Downstream Products

502186-10-9Relevant articles and documents

Anomeric α-azido acid (2-azido-2-deoxy-hept-2-ulopyranosonic acid) derivatives en route to peptides incorporating sugar amino acids

Czifrak, Katalin,Szilagyi, Peter,Somsak, Laszlo

, p. 127 - 141 (2007/10/03)

Per-O-acylated 2,6-anhydro-aldoheptonic acids of d-glycero-d-gulo and d-glycero-l-manno configuration obtained by nitrosation of the corresponding aldonamides were transformed into methyl-, tert-butyl-, 2,2,2-trichloroethyl-, and pentachlorophenyl esters,

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