Cas 1408321-12-9,2-(phenylmethoxy)-4-(phenylmethyl)-2,4-diazabicyclo[3.2.2]nonan-3-one

1408321-12-9

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Basic information

Product Name: 2-(phenylmethoxy)-4-(phenylmethyl)-2,4-diazabicyclo[3.2.2]nonan-3-one
Synonyms: 2-(phenylmethoxy)-4-(phenylmethyl)-2,4-diazabicyclo[3.2.2]nonan-3-one
CAS NO:1408321-12-9
Molecular Formula:
Molecular Weight: 336.434
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-(phenylmethoxy)-4-(phenylmethyl)-2,4-diazabicyclo[3.2.2]nonan-3-one(CAS DataBase Reference)
NIST Chemistry Reference: 2-(phenylmethoxy)-4-(phenylmethyl)-2,4-diazabicyclo[3.2.2]nonan-3-one(1408321-12-9)
EPA Substance Registry System: 2-(phenylmethoxy)-4-(phenylmethyl)-2,4-diazabicyclo[3.2.2]nonan-3-one(1408321-12-9)

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: 1408321-12-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1408321-12-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,8,3,2 and 1 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1408321-12:
(9*1)+(8*4)+(7*0)+(6*8)+(5*3)+(4*2)+(3*1)+(2*1)+(1*2)=119
119 % 10 = 9
So 1408321-12-9 is a valid CAS Registry Number.

1408321-12-9Upstream product

1408320-94-4 N-chloro-N-(phenylmethoxy)-N'-(phenylmethyl)urea

1408321-12-9Downstream Products

1408321-12-9Relevant academic research and scientific papers

1,4-diamination of cyclic dienes via a (4 + 3) cycloaddition of diaza-allyl cationic intermediates

Jeffrey, Christopher S.,Anumandla, Devendar,Carson, Christopher R.

, p. 5764 - 5767 (2013/01/15)

Diaza-(4 + 3) cycloadditions of putative diaza-oxyallyl cationic intermediates and cyclic dienes are reported as a method for the 1,4-diamination of cyclic dienes. This reaction was entirely selective for diamination and provided cycloadducts in good to excellent yield.

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