Cas 87357-92-4,(R)-3-[(1S,2R)-2-Benzyloxy-1-methoxy-2-((4S,5R)-2,2,5-trimethyl-[1,3]dioxolan-4-yl)-ethyl]-pent-4-enoic acid methyl ester

87357-92-4

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Basic information

Product Name: (R)-3-[(1S,2R)-2-Benzyloxy-1-methoxy-2-((4S,5R)-2,2,5-trimethyl-[1,3]dioxolan-4-yl)-ethyl]-pent-4-enoic acid methyl ester
Synonyms: (R)-3-[(1S,2R)-2-Benzyloxy-1-methoxy-2-((4S,5R)-2,2,5-trimethyl-[1,3]dioxolan-4-yl)-ethyl]-pent-4-enoic acid methyl ester
CAS NO:87357-92-4
Molecular Formula:
Molecular Weight: 392.492
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-((4S,5R)-2,2,5-trimethyl-[1,3]dioxolan-4-yl)-ethyl]-pent-4-enoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (R)-3-[(1S,2R)-2-Benzyloxy-1-methoxy-2-((4S,5R)-2,2,5-trimethyl-[1,3]dioxolan-4-yl)-ethyl]-pent-4-enoic acid methyl ester(87357-92-4)
EPA Substance Registry System: (R)-3-[(1S,2R)-2-Benzyloxy-1-methoxy-2-((4S,5R)-2,2,5-trimethyl-[1,3]dioxolan-4-yl)-ethyl]-pent-4-enoic acid methyl ester(87357-92-4)

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: 87357-92-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 87357-92-4 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 87357-92:
(7*8)+(6*7)+(5*3)+(4*5)+(3*7)+(2*9)+(1*2)=174
174 % 10 = 4
So 87357-92-4 is a valid CAS Registry Number.

87357-92-4Upstream product

120330-71-4 C₂₀H₂₈O₆

87357-92-4Downstream Products

87357-94-6 (R)-4-[(1S,2R)-2-Benzyloxy-1-methoxy-2-((4S,5R)-2,2,5-trimethyl-[1,3]dioxolan-4-yl)-ethyl]-2-methyl-hex-5-en-2-ol

87357-92-4Relevant 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 (1983)

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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