Cas 521315-85-5,Benzoic acid (2S,3R,5R)-5-ethoxycarbonylmethyl-2-iodomethyl-tetrahydro-furan-3-yl ester

521315-85-5

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Basic information

Product Name: Benzoic acid (2S,3R,5R)-5-ethoxycarbonylmethyl-2-iodomethyl-tetrahydro-furan-3-yl ester
Synonyms: Benzoic acid (2S,3R,5R)-5-ethoxycarbonylmethyl-2-iodomethyl-tetrahydro-furan-3-yl ester
CAS NO:521315-85-5
Molecular Formula:
Molecular Weight: 418.228
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: Benzoic acid (2S,3R,5R)-5-ethoxycarbonylmethyl-2-iodomethyl-tetrahydro-furan-3-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid (2S,3R,5R)-5-ethoxycarbonylmethyl-2-iodomethyl-tetrahydro-furan-3-yl ester(521315-85-5)
EPA Substance Registry System: Benzoic acid (2S,3R,5R)-5-ethoxycarbonylmethyl-2-iodomethyl-tetrahydro-furan-3-yl ester(521315-85-5)

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: 521315-85-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 521315-85-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,2,1,3,1 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 521315-85:
(8*5)+(7*2)+(6*1)+(5*3)+(4*1)+(3*5)+(2*8)+(1*5)=115
115 % 10 = 5
So 521315-85-5 is a valid CAS Registry Number.

521315-85-5Upstream product

521315-85-5Downstream Products

521315-87-7 Benzoic acid (1R,3R)-4-ethoxycarbonyl-3-hydroxy-1-vinyl-butyl ester

521315-85-5Relevant academic research and scientific papers

Synthesis of syn- and anti-3,5-dihydroxy-6-heptenoates from 2-deoxy-D-ribose: Intermediates for polyols synthesis

Zakrzewski, Peter,Lau, Cheuk K.

, p. 215 - 218 (2003)

Syntheses of all four diastereomers of syn- and anti-3,5-dihydroxy-6-heptenoate, proven versatile synthetic intermediates that are enantiomerically pure and functionally differentiated at both ends, have been developed.

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