Cas 85405-10-3,(R,S,R/S,R,S)-2-methyl-N<sup>1</sup>,1-diphenyl-3-p-tolyl-1,3-propanediamine

85405-10-3

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Basic information

Product Name: (R,S,R/S,R,S)-2-methyl-N¹,1-diphenyl-3-p-tolyl-1,3-propanediamine
Synonyms:
CAS NO:85405-10-3
Molecular Formula:
Molecular Weight: 330.473
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: (R,S,R/S,R,S)-2-methyl-N¹,1-diphenyl-3-p-tolyl-1,3-propanediamine(CAS DataBase Reference)
NIST Chemistry Reference: (R,S,R/S,R,S)-2-methyl-N¹,1-diphenyl-3-p-tolyl-1,3-propanediamine(85405-10-3)
EPA Substance Registry System: (R,S,R/S,R,S)-2-methyl-N¹,1-diphenyl-3-p-tolyl-1,3-propanediamine(85405-10-3)

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: 85405-10-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 85405-10-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,4,0 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 85405-10:
(7*8)+(6*5)+(5*4)+(4*0)+(3*5)+(2*1)+(1*0)=123
123 % 10 = 3
So 85405-10-3 is a valid CAS Registry Number.

85405-10-3Upstream product

54080-00-1 [3-Imino-2-methyl-1-phenyl-3-p-tolyl-prop-(E)-ylidene]-phenyl-amine

85405-10-3Downstream Products

85405-10-3Relevant academic research and scientific papers

Reduction of 1,3-Diimines. A New and General Method of Synthesis of γ-Diamines, β-Amino Ketones, and Derivatives with Two and Three Chiral Centers

Barluenga, Jose,Olano, Bernardo,Fustero, Santos

, p. 2255 - 2259 (2007/10/02)

1,3-Diimes 1 are easily reduced with Na/i-PrOH to afford unsymmetrical N-substituted γ-diamines 8 in nearly quantitative yields.Since three chiral centers are generated, compounds 8 are isolated as a mixture of diastereoisomers which are easily separated.

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