Cas 80403-49-2,(3R,5S)-3-Hydroxy-4,4-dimethyl-7-oxo-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid; compound with 2,2,4a,7,7-pentamethyl-1,2,3,4,4a,5,6,7-octahydro-[1,8]naphthyridine

80403-49-2

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Basic information

Product Name: (3R,5S)-3-Hydroxy-4,4-dimethyl-7-oxo-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid; compound with 2,2,4a,7,7-pentamethyl-1,2,3,4,4a,5,6,7-octahydro-[1,8]naphthyridine
Synonyms:
CAS NO:80403-49-2
Molecular Formula:
Molecular Weight: 407.553
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: (3R,5S)-3-Hydroxy-4,4-dimethyl-7-oxo-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid; compound with 2,2,4a,7,7-pentamethyl-1,2,3,4,4a,5,6,7-octahydro-[1,8]naphthyridine(CAS DataBase Reference)
NIST Chemistry Reference: (3R,5S)-3-Hydroxy-4,4-dimethyl-7-oxo-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid; compound with 2,2,4a,7,7-pentamethyl-1,2,3,4,4a,5,6,7-octahydro-[1,8]naphthyridine(80403-49-2)
EPA Substance Registry System: (3R,5S)-3-Hydroxy-4,4-dimethyl-7-oxo-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid; compound with 2,2,4a,7,7-pentamethyl-1,2,3,4,4a,5,6,7-octahydro-[1,8]naphthyridine(80403-49-2)

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: 80403-49-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 80403-49-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,4,0 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 80403-49:
(7*8)+(6*0)+(5*4)+(4*0)+(3*3)+(2*4)+(1*9)=102
102 % 10 = 2
So 80403-49-2 is a valid CAS Registry Number.

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80403-49-2Relevant academic research and scientific papers

SYNTHESIS OF 1,1-DIMETHYLCARBA-2-PENEM DERIVATIVES VIA A DIECKMANN-TYPE CYCLIZATION

Shibuya, Masayuki,Kubota, Seiju

, p. 3611 - 3614 (1981)

The synthesis of 1,1-dimethylcarba-2-penem derivatives via a Dieckmann-type cyclization and the use of a new method for removing the benzyl protecting group are reported.

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