Cas 87357-96-8,(R)-3-[(1S,2R)-2-Benzyloxy-1-methoxy-2-((2S,3R)-3-methyl-1,4-dioxa-spiro[4.5]dec-2-yl)-ethyl]-pent-4-enoic acid ethyl ester

87357-96-8

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Basic information

Product Name: (R)-3-[(1S,2R)-2-Benzyloxy-1-methoxy-2-((2S,3R)-3-methyl-1,4-dioxa-spiro[4.5]dec-2-yl)-ethyl]-pent-4-enoic acid ethyl ester
Synonyms:
CAS NO:87357-96-8
Molecular Formula:
Molecular Weight: 446.584
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: (R)-3-[(1S,2R)-2-Benzyloxy-1-methoxy-2-((2S,3R)-3-methyl-1,4-dioxa-spiro[4.5]dec-2-yl)-ethyl]-pent-4-enoic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (R)-3-[(1S,2R)-2-Benzyloxy-1-methoxy-2-((2S,3R)-3-methyl-1,4-dioxa-spiro[4.5]dec-2-yl)-ethyl]-pent-4-enoic acid ethyl ester(87357-96-8)
EPA Substance Registry System: (R)-3-[(1S,2R)-2-Benzyloxy-1-methoxy-2-((2S,3R)-3-methyl-1,4-dioxa-spiro[4.5]dec-2-yl)-ethyl]-pent-4-enoic acid ethyl ester(87357-96-8)

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: 87357-96-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 87357-96-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,3,5 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 87357-96:
(7*8)+(6*7)+(5*3)+(4*5)+(3*7)+(2*9)+(1*6)=178
178 % 10 = 8
So 87357-96-8 is a valid CAS Registry Number.

87357-96-8Upstream product

120329-89-7 Ethyl D-galacto-5-(benzyloxy)-6,7-dihydroxy-4-methoxyoct-2(E)-enoate 6,7-cyclohexyl ketal

87357-96-8Downstream Products

87357-96-8Relevant academic research and scientific papers

Stereochemistry of Vinyl Cuprate Additions to Carbohydrate-Derived Enones and α,β-Unsaturated Esters

Roush, William R.,Lesur, Brigitte M.

, p. 2231 - 2234 (2007/10/02)

Vinylic cuprate reagents add with excellent diastereoselectivity (>10:1) to carbohydrate derived enones and α,β-unsaturated esters.The stereochemical outcome of these transformations is consistent with a Felkin-type addition pathway.

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