Cas 728040-97-9,(1S)-2-[(1H-1,2,3-benzotriazol-1-yl)methyl]-1-phenyl-2,3-dihydro-1H-naphtho[1,2-e][1,3]oxazine

728040-97-9

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Basic information

Product Name: (1S)-2-[(1H-1,2,3-benzotriazol-1-yl)methyl]-1-phenyl-2,3-dihydro-1H-naphtho[1,2-e][1,3]oxazine
Synonyms: (1S)-2-[(1H-1,2,3-benzotriazol-1-yl)methyl]-1-phenyl-2,3-dihydro-1H-naphtho[1,2-e][1,3]oxazine
CAS NO:728040-97-9
Molecular Formula:
Molecular Weight: 392.46
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: (1S)-2-[(1H-1,2,3-benzotriazol-1-yl)methyl]-1-phenyl-2,3-dihydro-1H-naphtho[1,2-e][1,3]oxazine(CAS DataBase Reference)
NIST Chemistry Reference: (1S)-2-[(1H-1,2,3-benzotriazol-1-yl)methyl]-1-phenyl-2,3-dihydro-1H-naphtho[1,2-e][1,3]oxazine(728040-97-9)
EPA Substance Registry System: (1S)-2-[(1H-1,2,3-benzotriazol-1-yl)methyl]-1-phenyl-2,3-dihydro-1H-naphtho[1,2-e][1,3]oxazine(728040-97-9)

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: 728040-97-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 728040-97-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,8,0,4 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 728040-97:
(8*7)+(7*2)+(6*8)+(5*0)+(4*4)+(3*0)+(2*9)+(1*7)=159
159 % 10 = 9
So 728040-97-9 is a valid CAS Registry Number.

728040-97-9Upstream product

728040-97-9Downstream Products

219897-59-3 (S)-1-[(dimethylamino)(phenyl)methyl]-2-naphthol

728040-97-9Relevant academic research and scientific papers

Highly regioselective N-alkylation of nonracemic Betti base: A novel one-pot synthesis of chiral N-methyl-N-alkyl Betti bases

Dong, Yanmei,Sun, Jianwei,Wang, Xinyan,Xu, Xuenong,Cao, Liya,Hu, Yuefei

, p. 1667 - 1672 (2007/10/03)

A novel one-pot preparation of chiral N-methyl-N-alkyl Betti bases has been developed involving a highly regioselective N-alkylation of (S)-(+)-Betti base. The strategy involved formation-cleavage of the oxazine ring and N-methylation with BtCH2/sub

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