Cas 129094-30-0,Acetic acid (2R,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-benzenesulfonyl-2-bromo-tetrahydro-pyran-3-yl ester

129094-30-0

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Basic information

Product Name: Acetic acid (2R,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-benzenesulfonyl-2-bromo-tetrahydro-pyran-3-yl ester
Synonyms:
CAS NO:129094-30-0
Molecular Formula:
Molecular Weight: 551.366
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: Acetic acid (2R,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-benzenesulfonyl-2-bromo-tetrahydro-pyran-3-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (2R,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-benzenesulfonyl-2-bromo-tetrahydro-pyran-3-yl ester(129094-30-0)
EPA Substance Registry System: Acetic acid (2R,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-benzenesulfonyl-2-bromo-tetrahydro-pyran-3-yl ester(129094-30-0)

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: 129094-30-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 129094-30-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,0,9 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 129094-30:
(8*1)+(7*2)+(6*9)+(5*0)+(4*9)+(3*4)+(2*3)+(1*0)=130
130 % 10 = 0
So 129094-30-0 is a valid CAS Registry Number.

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129094-30-0Relevant academic research and scientific papers

Comparative photohalogenation of phenylglucopyranoside and its oxidation derivatives

Praly,Descotes

, p. 1133 - 1136 (2007/10/02)

The photobrominations of the peracetylated phenyl thio-1-β-D-glucopyranoside and of the corresponding sulphoxides and sulphone have been investigated. The differences observed in both substrate reactivity and substitution regioselectivity indicate an easier homolysis of the anomeric C-H bond in the thioglycoside.

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