Cas 1258684-23-9,3-(4-methoxyphenyl)-2-(11-methylamino-1,4-dioxa-9-azadispiro[4.2.4.2]tetradec-9-yl)-propan-1-ol

1258684-23-9

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Basic information

Product Name: 3-(4-methoxyphenyl)-2-(11-methylamino-1,4-dioxa-9-azadispiro[4.2.4.2]tetradec-9-yl)-propan-1-ol
Synonyms: 3-(4-methoxyphenyl)-2-(11-methylamino-1,4-dioxa-9-azadispiro[4.2.4.2]tetradec-9-yl)-propan-1-ol
CAS NO:1258684-23-9
Molecular Formula:
Molecular Weight: 390.523
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: 3-(4-methoxyphenyl)-2-(11-methylamino-1,4-dioxa-9-azadispiro[4.2.4.2]tetradec-9-yl)-propan-1-ol(CAS DataBase Reference)
NIST Chemistry Reference: 3-(4-methoxyphenyl)-2-(11-methylamino-1,4-dioxa-9-azadispiro[4.2.4.2]tetradec-9-yl)-propan-1-ol(1258684-23-9)
EPA Substance Registry System: 3-(4-methoxyphenyl)-2-(11-methylamino-1,4-dioxa-9-azadispiro[4.2.4.2]tetradec-9-yl)-propan-1-ol(1258684-23-9)

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: 1258684-23-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1258684-23-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,8,6,8 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1258684-23:
(9*1)+(8*2)+(7*5)+(6*8)+(5*6)+(4*8)+(3*4)+(2*2)+(1*3)=189
189 % 10 = 9
So 1258684-23-9 is a valid CAS Registry Number.

1258684-23-9Upstream product

1258684-48-8 2-[11-(benzylmethylamino)-1,4-dioxa-9-azadispiro[4.2.4.2]tetradec-9-yl]-3-(4-methoxyphenyl)-propan-1-ol

1258684-23-9Downstream Products

1258684-29-5 (5S)-4-methyl-2-[(4-methoxyphenyl)methyl]-dispiro-[1,4-diazabicyclo[3.2.1]oct[2]en-7,1'-cyclohexane-4',2-[1,3]dioxepane]

1258684-23-9Relevant academic research and scientific papers

Enantioselective synthesis of the diazatricyclic core of alkaloid TAN1251C via an iodoaminocyclization reaction

Zhang, Hongkui,Lin, Zhijie,Huang, Huang,Huo, Haohua,Huang, Yanju,Ye, Jianliang,Huang, Peiqiang

, p. 1717 - 1724 (2011/07/31)

A concise enantioselective synthesis of the diazatricyclic core of alkaloid TAN1251C is reported. The method featured a stereoselective formation of the iodide intermediate 16b (in 2:1 ratio) from homoallylic amine 11b by iodine-promoted iodoaminocyclizat

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