Cas 794580-66-8,(Z)-4-[(2S,3S)-3-((R)-Hydroxy-phenyl-methyl)-oxiranyl]-but-2-enoic acid methyl ester

794580-66-8

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Basic information

Product Name: (Z)-4-[(2S,3S)-3-((R)-Hydroxy-phenyl-methyl)-oxiranyl]-but-2-enoic acid methyl ester
Synonyms: (Z)-4-[(2S,3S)-3-((R)-Hydroxy-phenyl-methyl)-oxiranyl]-but-2-enoic acid methyl ester
CAS NO:794580-66-8
Molecular Formula:
Molecular Weight: 248.279
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: (Z)-4-[(2S,3S)-3-((R)-Hydroxy-phenyl-methyl)-oxiranyl]-but-2-enoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-4-[(2S,3S)-3-((R)-Hydroxy-phenyl-methyl)-oxiranyl]-but-2-enoic acid methyl ester(794580-66-8)
EPA Substance Registry System: (Z)-4-[(2S,3S)-3-((R)-Hydroxy-phenyl-methyl)-oxiranyl]-but-2-enoic acid methyl ester(794580-66-8)

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: 794580-66-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 794580-66-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,4,5,8 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 794580-66:
(8*7)+(7*9)+(6*4)+(5*5)+(4*8)+(3*0)+(2*6)+(1*6)=218
218 % 10 = 8
So 794580-66-8 is a valid CAS Registry Number.

794580-66-8Upstream product

473980-85-7 (2Z,5E)-(S)-7-Hydroxy-7-phenyl-hepta-2,5-dienoic acid methyl ester

794580-66-8Downstream Products

794580-66-8Relevant academic research and scientific papers

Stereoselective synthesis of the styryllactones, 7-epi-goniodiol and leiocarpin A, isolated from Goniothalamus leiocarpus

Chen, Jian,Lin, Guo-Qiang,Liu, Han-Quan

, p. 8111 - 8113 (2004)

Two novel styryllactones, 7-epi-goniodiol and leiocarpin A, isolated from Goniothalamus leiocarpus, were stereoselectively synthesized in a short and efficient route from cinnamyl alcohol based on the asymmetric epoxidation and the palladium-catalyzed cross-coupling of vinyl epoxide with vinyltributylstannane.

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