Cas 1303531-29-4,(R)-(-)-4-hydroxy-6-((3-methylbutanoyloxy)(phenyl)methyl)-2-oxo-1,2-dihydropyridine-3-carboxylic acid

1303531-29-4

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Basic information

Product Name: (R)-(-)-4-hydroxy-6-((3-methylbutanoyloxy)(phenyl)methyl)-2-oxo-1,2-dihydropyridine-3-carboxylic acid
Synonyms: (R)-(-)-4-hydroxy-6-((3-methylbutanoyloxy)(phenyl)methyl)-2-oxo-1,2-dihydropyridine-3-carboxylic acid
CAS NO:1303531-29-4
Molecular Formula:
Molecular Weight: 345.352
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)-(-)-4-hydroxy-6-((3-methylbutanoyloxy)(phenyl)methyl)-2-oxo-1,2-dihydropyridine-3-carboxylic acid(CAS DataBase Reference)
NIST Chemistry Reference: (R)-(-)-4-hydroxy-6-((3-methylbutanoyloxy)(phenyl)methyl)-2-oxo-1,2-dihydropyridine-3-carboxylic acid(1303531-29-4)
EPA Substance Registry System: (R)-(-)-4-hydroxy-6-((3-methylbutanoyloxy)(phenyl)methyl)-2-oxo-1,2-dihydropyridine-3-carboxylic acid(1303531-29-4)

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: 1303531-29-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1303531-29-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,3,5,3 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1303531-29:
(9*1)+(8*3)+(7*0)+(6*3)+(5*5)+(4*3)+(3*1)+(2*2)+(1*9)=104
104 % 10 = 4
So 1303531-29-4 is a valid CAS Registry Number.

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1303531-29-4Relevant academic research and scientific papers

SPF32629A and SPF32629B: Enantioselective synthesis, determination of absolute configuration, cytotoxicity and antibacterial evaluation

Vegi, Srinivasa Rao,Boovanahalli, Shanthaveerappa K.,Patro, Balaram,Mukkanti

, p. 1803 - 1812 (2011/05/07)

We report herein an efficient enantioselective synthesis of SPF32629A and SPF32629B through one-pot enantioselective reduction and protecting-group-free regioselective O-acylation strategy. The absolute configuration of the enantiomerically pure isomers w

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