Cas 20002-23-7,N-nitroso<α,α,α'α'-2H4>dibenzylamine

20002-23-7

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Basic information

Product Name: N-nitroso<α,α,α'α'-2H4>dibenzylamine
Synonyms: N-nitroso<α,α,α'α'-2H4>dibenzylamine
CAS NO:20002-23-7
Molecular Formula:
Molecular Weight: 230.246
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: N-nitroso<α,α,α'α'-2H4>dibenzylamine(CAS DataBase Reference)
NIST Chemistry Reference: N-nitroso<α,α,α'α'-2H4>dibenzylamine(20002-23-7)
EPA Substance Registry System: N-nitroso<α,α,α'α'-2H4>dibenzylamine(20002-23-7)

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: 20002-23-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 20002-23-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,0,0 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 20002-23:
(7*2)+(6*0)+(5*0)+(4*0)+(3*2)+(2*2)+(1*3)=27
27 % 10 = 7
So 20002-23-7 is a valid CAS Registry Number.

20002-23-7Upstream product

20002-23-7Downstream Products

3592-47-0 Benzaldehyde-d

20002-23-7Relevant academic research and scientific papers

Oxidation of N-Nitrosodibenzylamine and Related Compounds by Metalloporphyrin-catalysed Model Systems for the Cytochrome P450 Dependent Mono-oxygenases

Smith, John R. Lindsay,Nee, Michael W.,Noar, J. Barry,Bruice, Thomas C.

, p. 255 - 260 (2007/10/02)

N-Nitrosodibenzylamine has been oxidised to benzaldehyde and benzyl alcohol by iodosylbenzene, 3-chloroperoxybenzoic acid and t-butyl hydroperoxide catalysed by tetraphenylporphyrinato-iron(III) chloride or -manganese(III) chloride.The influence of reaction conditions on the product yields and distribution have been studied.Kinetic isotope effects have been measured with deuteriated N-nitrosodibenzylamines for inter- and intra-molecular competition for the oxidants.The evidence presented is in favour of the iodosylbenzene and t-butyl hydroperoxide oxidations being initiated by hydrogen-atom abstraction by the oxidant from the α-hydrogen of the benzyl group.However, oxidations by the peroxy acid systems may proceed by an initial electron transfer.The reactions of N-nitrosodimethylamine and N-nitrosopiperidine with the metalloporphyrin-catalysed systems show that these substrates are surprisingly unreactive towards oxidation.

Investigations on the Aprotic Deamination of Benzylamine and (α,α-2H2)Benzylamine

Bakke, Ian M.,Svendsen, K.

, p. 179 - 184 (2007/10/02)

The reaction of benzylamine with nitrosyl chloride in diethyl ether at -50 deg C gave diazotoluene (16percent), benzyl alcohol (15percent), benzyl chloride (31percent) and α,α-azoxytoluene (12percent) together with several other products.The same reaction

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