Cas 87614-44-6,2,4,6-Trimethyl-benzenesulfonic acid (2S,3R,4R,5R)-3,4-dihydroxy-5-methoxy-tetrahydro-furan-2-ylmethyl ester

87614-44-6

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Basic information

Product Name: 2,4,6-Trimethyl-benzenesulfonic acid (2S,3R,4R,5R)-3,4-dihydroxy-5-methoxy-tetrahydro-furan-2-ylmethyl ester
Synonyms: 2,4,6-Trimethyl-benzenesulfonic acid (2S,3R,4R,5R)-3,4-dihydroxy-5-methoxy-tetrahydro-furan-2-ylmethyl ester
CAS NO:87614-44-6
Molecular Formula:
Molecular Weight: 346.401
EINECS: N/A
Product Categories: N/A
Mol File: 87614-44-6.mol
Article Data: 1

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: 2,4,6-Trimethyl-benzenesulfonic acid (2S,3R,4R,5R)-3,4-dihydroxy-5-methoxy-tetrahydro-furan-2-ylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2,4,6-Trimethyl-benzenesulfonic acid (2S,3R,4R,5R)-3,4-dihydroxy-5-methoxy-tetrahydro-furan-2-ylmethyl ester(87614-44-6)
EPA Substance Registry System: 2,4,6-Trimethyl-benzenesulfonic acid (2S,3R,4R,5R)-3,4-dihydroxy-5-methoxy-tetrahydro-furan-2-ylmethyl ester(87614-44-6)

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: 87614-44-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 87614-44-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,6,1 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 87614-44:
(7*8)+(6*7)+(5*6)+(4*1)+(3*4)+(2*4)+(1*4)=156
156 % 10 = 6
So 87614-44-6 is a valid CAS Registry Number.

87614-44-6Upstream product

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87614-44-6Relevant articles and documents

ENANTIOSPECIFIC SYNTHESIS OF (3S-HYDROXY-2S-METHYL)BUTYLTRIPHENYLPHOSPHONIUM IODIDE, A PRECURSOR FOR THE CHIRAL SIDE CHAIN OF PSEUDOMONIC ACID C

Fleet, G. W. J.,Shing, T. K. M.

, p. 3657 - 3660 (2007/10/02)

The enantiospecific synthesis of (3S-hydroxy-2S-methyl)butyltriphenylphosphonium iodide from L-arabinose is described.

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