Cas 98442-30-9,(5aR,9aS,11aS)-5a-benzyl-1,2,3,8,9,9a,10,11,11a-nonahydro-5H-pyrrolo<2,1-c><1,4>benzodiazepine-5,11-dione

98442-30-9

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Basic information

Product Name: (5aR,9aS,11aS)-5a-benzyl-1,2,3,8,9,9a,10,11,11a-nonahydro-5H-pyrrolo<2,1-c><1,4>benzodiazepine-5,11-dione
Synonyms: (5aR,9aS,11aS)-5a-benzyl-1,2,3,8,9,9a,10,11,11a-nonahydro-5H-pyrrolo<2,1-c><1,4>benzodiazepine-5,11-dione
CAS NO:98442-30-9
Molecular Formula:
Molecular Weight: 310.396
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: (5aR,9aS,11aS)-5a-benzyl-1,2,3,8,9,9a,10,11,11a-nonahydro-5H-pyrrolo<2,1-c><1,4>benzodiazepine-5,11-dione(CAS DataBase Reference)
NIST Chemistry Reference: (5aR,9aS,11aS)-5a-benzyl-1,2,3,8,9,9a,10,11,11a-nonahydro-5H-pyrrolo<2,1-c><1,4>benzodiazepine-5,11-dione(98442-30-9)
EPA Substance Registry System: (5aR,9aS,11aS)-5a-benzyl-1,2,3,8,9,9a,10,11,11a-nonahydro-5H-pyrrolo<2,1-c><1,4>benzodiazepine-5,11-dione(98442-30-9)

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: 98442-30-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 98442-30-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,4,4 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 98442-30:
(7*9)+(6*8)+(5*4)+(4*4)+(3*2)+(2*3)+(1*0)=159
159 % 10 = 9
So 98442-30-9 is a valid CAS Registry Number.

98442-30-9Upstream product

98442-30-9Downstream Products

98442-35-4 (1R,4R,5S)-4-benzyl-5-amino-2-oxabicyclo<3,2,1>octan-3-one

98442-30-9Relevant academic research and scientific papers

ENANTIOSELECTION VIA BIRCH REDUCTION-ALKYLATION OF A CHIRAL ANTHRANILIC ACID DERIVATIVE. SYNTHESIS OF ENANTIOMERICALLY PURE AMINOCYCLOHEXANES

Schultz, Arthur G.,McCloskey, Patrick J.,Sundararaman, Padmanabhan,Springer, James P.

, p. 1619 - 1622 (2007/10/02)

The first method for preparation of enantiomerically pure aminocyclohexanes by Birch reduction-alkylation of a chiral anthranilic acid derivative is described; stereochemistry of alkylation is demonstrated by X-ray structural studies with 2b.

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