Cas 613681-75-7,((2R,3R,4R,5S,6S)-3,4,5-Tris-benzyloxy-2-hydroxy-6-methyl-tetrahydro-pyran-2-yl)-acetic acid tert-butyl ester

613681-75-7

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Basic information

Product Name: ((2R,3R,4R,5S,6S)-3,4,5-Tris-benzyloxy-2-hydroxy-6-methyl-tetrahydro-pyran-2-yl)-acetic acid tert-butyl ester
Synonyms: ((2R,3R,4R,5S,6S)-3,4,5-Tris-benzyloxy-2-hydroxy-6-methyl-tetrahydro-pyran-2-yl)-acetic acid tert-butyl ester
CAS NO:613681-75-7
Molecular Formula:
Molecular Weight: 548.676
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: ((2R,3R,4R,5S,6S)-3,4,5-Tris-benzyloxy-2-hydroxy-6-methyl-tetrahydro-pyran-2-yl)-acetic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: ((2R,3R,4R,5S,6S)-3,4,5-Tris-benzyloxy-2-hydroxy-6-methyl-tetrahydro-pyran-2-yl)-acetic acid tert-butyl ester(613681-75-7)
EPA Substance Registry System: ((2R,3R,4R,5S,6S)-3,4,5-Tris-benzyloxy-2-hydroxy-6-methyl-tetrahydro-pyran-2-yl)-acetic acid tert-butyl ester(613681-75-7)

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: 613681-75-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 613681-75-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,3,6,8 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 613681-75:
(8*6)+(7*1)+(6*3)+(5*6)+(4*8)+(3*1)+(2*7)+(1*5)=157
157 % 10 = 7
So 613681-75-7 is a valid CAS Registry Number.

613681-75-7Upstream product

613681-75-7Downstream Products

613681-75-7Relevant academic research and scientific papers

A new Co(0) complex mediated synthesis of C-glycoside analogues

Orsini, Fulvia,Di Teodoro, Emanuela

, p. 2521 - 2528 (2003)

Properly protected glyconolactones, readily available from the parent sugars, react under mild conditions with α-bromoacetates in the presence of a soluble Co(0) complex, either in stoichiometric or substoichiometric amounts, to give a Reformatsky-type addition product to the lactone. The addition product can be subsequently converted into a variety of compounds: dehydroxylation with triethylsilane in the presence of boron trifluoride affords C-glycosides.

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