Cas 676530-91-9,2-Azidomethyl-benzoic acid (2S,3R,4S,5R,6R)-2-allyloxy-4-benzoyloxy-5-hydroxy-6-hydroxymethyl-tetrahydro-pyran-3-yl ester

676530-91-9

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Basic information

Product Name: 2-Azidomethyl-benzoic acid (2S,3R,4S,5R,6R)-2-allyloxy-4-benzoyloxy-5-hydroxy-6-hydroxymethyl-tetrahydro-pyran-3-yl ester
Synonyms: 2-Azidomethyl-benzoic acid (2S,3R,4S,5R,6R)-2-allyloxy-4-benzoyloxy-5-hydroxy-6-hydroxymethyl-tetrahydro-pyran-3-yl ester
CAS NO:676530-91-9
Molecular Formula:
Molecular Weight: 483.478
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: 2-Azidomethyl-benzoic acid (2S,3R,4S,5R,6R)-2-allyloxy-4-benzoyloxy-5-hydroxy-6-hydroxymethyl-tetrahydro-pyran-3-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-Azidomethyl-benzoic acid (2S,3R,4S,5R,6R)-2-allyloxy-4-benzoyloxy-5-hydroxy-6-hydroxymethyl-tetrahydro-pyran-3-yl ester(676530-91-9)
EPA Substance Registry System: 2-Azidomethyl-benzoic acid (2S,3R,4S,5R,6R)-2-allyloxy-4-benzoyloxy-5-hydroxy-6-hydroxymethyl-tetrahydro-pyran-3-yl ester(676530-91-9)

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: 676530-91-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 676530-91-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,6,5,3 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 676530-91:
(8*6)+(7*7)+(6*6)+(5*5)+(4*3)+(3*0)+(2*9)+(1*1)=189
189 % 10 = 9
So 676530-91-9 is a valid CAS Registry Number.

676530-91-9Upstream product

676530-91-9Downstream Products

676530-78-2 allyl 4,6-di-O-acetyl-2-O-(2-azidomethyl)benzoyl-3-O-benzoyl-α-D-glucopyranoside

676530-91-9Relevant academic research and scientific papers

Facile Synthesis of Ginsenoside Ro

Peng, Wenjie,Sun, Jiansong,Lin, Feng,Han, Xiuwen,Yu, Biao

, p. 259 - 262 (2007/10/03)

Two concise synthetic routes, being different in the glycosylation sequence, toward ginsenoside Ro (1) are developed. These syntheses feature the elaboration of the glucuronide residue at a later stage via the TEMPO-mediated selective oxidation and the installation of AZMB as a benzoylic neighboring participating group capable of being selectively removed afterward.

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