Cas 76524-14-6,(3aR,4R,6aR)-2-Amino-4-ethyl-6-oxo-3a,4,6,6a-tetrahydro-furo[3,4-b]furan-3-carboxylic acid 4-methoxy-benzyl ester

76524-14-6

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Basic information

Product Name: (3aR,4R,6aR)-2-Amino-4-ethyl-6-oxo-3a,4,6,6a-tetrahydro-furo[3,4-b]furan-3-carboxylic acid 4-methoxy-benzyl ester
Synonyms: (3aR,4R,6aR)-2-Amino-4-ethyl-6-oxo-3a,4,6,6a-tetrahydro-furo[3,4-b]furan-3-carboxylic acid 4-methoxy-benzyl ester
CAS NO:76524-14-6
Molecular Formula:
Molecular Weight: 333.341
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: (3aR,4R,6aR)-2-Amino-4-ethyl-6-oxo-3a,4,6,6a-tetrahydro-furo[3,4-b]furan-3-carboxylic acid 4-methoxy-benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (3aR,4R,6aR)-2-Amino-4-ethyl-6-oxo-3a,4,6,6a-tetrahydro-furo[3,4-b]furan-3-carboxylic acid 4-methoxy-benzyl ester(76524-14-6)
EPA Substance Registry System: (3aR,4R,6aR)-2-Amino-4-ethyl-6-oxo-3a,4,6,6a-tetrahydro-furo[3,4-b]furan-3-carboxylic acid 4-methoxy-benzyl ester(76524-14-6)

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: 76524-14-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 76524-14-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,5,2 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 76524-14:
(7*7)+(6*6)+(5*5)+(4*2)+(3*4)+(2*1)+(1*4)=136
136 % 10 = 6
So 76524-14-6 is a valid CAS Registry Number.

76524-14-6Upstream product

76524-14-6Downstream Products

33644-10-9 epi-ethisolide

76524-14-6Relevant academic research and scientific papers

TOTAL SYNTHESIS OF (+/-)-AVENACIOLIDE AND ITS ANALOGUES

Takei, Hisashi,Fukuda, Yoshimasa,Taguchi, Takeo,Kawara, Tatsuo,Mizutani, Hidemi,Mukuta, Takashi

, p. 1311 - 1314 (2007/10/02)

A new method for the stereoselective synthesis of (+/-)-avenaciolide and its analogues via methoxycarbonyl- or anisyloxycarbonyldi-γ-lactones, which could be easily prepared by the reaction of γ-substituted α-bromobutenolides with sodium salt of methyl or anisyl malonamate in good yields, was described.

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