Cas 81310-22-7,2,2,4a,7,7-Pentamethyl-1,2,3,4,4a,5,6,7-octahydro-[1,8]naphthyridine; compound with (2R,5R)-3,3-dimethyl-7-oxo-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid

81310-22-7

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Basic information

Product Name: 2,2,4a,7,7-Pentamethyl-1,2,3,4,4a,5,6,7-octahydro-[1,8]naphthyridine; compound with (2R,5R)-3,3-dimethyl-7-oxo-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid
Synonyms:
CAS NO:81310-22-7
Molecular Formula:
Molecular Weight: 391.554
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: 2,2,4a,7,7-Pentamethyl-1,2,3,4,4a,5,6,7-octahydro-[1,8]naphthyridine; compound with (2R,5R)-3,3-dimethyl-7-oxo-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid(CAS DataBase Reference)
NIST Chemistry Reference: 2,2,4a,7,7-Pentamethyl-1,2,3,4,4a,5,6,7-octahydro-[1,8]naphthyridine; compound with (2R,5R)-3,3-dimethyl-7-oxo-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid(81310-22-7)
EPA Substance Registry System: 2,2,4a,7,7-Pentamethyl-1,2,3,4,4a,5,6,7-octahydro-[1,8]naphthyridine; compound with (2R,5R)-3,3-dimethyl-7-oxo-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid(81310-22-7)

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: 81310-22-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 81310-22-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,3,1 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 81310-22:
(7*8)+(6*1)+(5*3)+(4*1)+(3*0)+(2*2)+(1*2)=87
87 % 10 = 7
So 81310-22-7 is a valid CAS Registry Number.

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81310-22-7Relevant academic research and scientific papers

SYNTHESIS OF 2,2-DIMETHYL-1-CARBAPENAM DERIVATIVES VIA AN INTRAMOLECULAR MICHAEL-TYPE REACTION

Shibuya, Masayuki,Kuretani, Masahiko,Kubota, Seiju

, p. 4453 - 4456 (1981)

The synthesis of 2,2-dimethyl-1-carbapenam derivatives via an intramolecular Michael-type condensation reaction is described.

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