Cas 1003300-75-1,methyl (S)-3-[(2S,3S,4S,5R)-3,4-dihydroxy-5-phenyltetrahydrofuran-2-yl]-3-hydroxypropanoate

1003300-75-1

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Basic information

Product Name: methyl (S)-3-[(2S,3S,4S,5R)-3,4-dihydroxy-5-phenyltetrahydrofuran-2-yl]-3-hydroxypropanoate
Synonyms: methyl (S)-3-[(2S,3S,4S,5R)-3,4-dihydroxy-5-phenyltetrahydrofuran-2-yl]-3-hydroxypropanoate
CAS NO:1003300-75-1
Molecular Formula:
Molecular Weight: 282.293
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: methyl (S)-3-[(2S,3S,4S,5R)-3,4-dihydroxy-5-phenyltetrahydrofuran-2-yl]-3-hydroxypropanoate(CAS DataBase Reference)
NIST Chemistry Reference: methyl (S)-3-[(2S,3S,4S,5R)-3,4-dihydroxy-5-phenyltetrahydrofuran-2-yl]-3-hydroxypropanoate(1003300-75-1)
EPA Substance Registry System: methyl (S)-3-[(2S,3S,4S,5R)-3,4-dihydroxy-5-phenyltetrahydrofuran-2-yl]-3-hydroxypropanoate(1003300-75-1)

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: 1003300-75-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1003300-75-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,3,3,0 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1003300-75:
(9*1)+(8*0)+(7*0)+(6*3)+(5*3)+(4*0)+(3*0)+(2*7)+(1*5)=61
61 % 10 = 1
So 1003300-75-1 is a valid CAS Registry Number.

1003300-75-1Upstream product

1002753-36-7 methyl (S)-3-[(2S,3R,4R,5R)-3,4-bis(tert-butyldimethylsiloxy)-5-phenyltetrahydrofuran-2-yl]-3-hydroxypropanoate

1003300-75-1Downstream Products

1003300-75-1Relevant academic research and scientific papers

First total synthesis and absolute configuration of the styryl lactone gonioheptolide A

Gupta, Shuchi,Rajagopalan, Murali,Alhamadsheh, Mamoun M.,Tillekeratne, L. M. Viranga,Hudson, Richard A.

, p. 3512 - 3518 (2008/09/20)

Efficient asymmetric syntheses of both naturally occurring and non-naturally occurring enantiomers of gonioheptolide A are reported. The absolute configuration of (+)-gonioheptolide A was established by NOESY, Mosher ester analysis, and comparison with the specific rotation of the isolated (+)-gonioheptolide A. Georg Thieme Verlag Stuttgart.

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