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N,N'-dibenzyl-2,3-diaminobutane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75825-39-7

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75825-39-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75825-39-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,8,2 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75825-39:
(7*7)+(6*5)+(5*8)+(4*2)+(3*5)+(2*3)+(1*9)=157
157 % 10 = 7
So 75825-39-7 is a valid CAS Registry Number.

75825-39-7Relevant academic research and scientific papers

Preparation of racemic 2,3-diaminobutane and the resolution of its (2S,3S) enantiomer

Scaros, Mike G.,Yonan, Peter K.,Laneman, Scott A.,Fernando, Peter N.

, p. 1501 - 1506 (1997)

A three-step procedure for large scale preparation of pure racemic 2,3-diaminobutane from relatively inexpensive meso 2,3-butanediol is described. Also, an efficient method for the resolution of (S,S) 2,3-diaminobutane from the racemic mixture in 95% ee has been developed.

Novel reductive coupling of aldimines to vicinal diamines

Baruah, Bipul

, p. 6747 - 6750 (2007/10/02)

Reductive coupling of aldimines into vicinal diamines has been performed by the action of aluminium/bismuth powder and potassium hydroxide in methanol at ambient temperature in high yields.

Titanium Induced Coupling of Imines to Symmetrical Vicinal (R*,R*)-Diamines

Mangeney, P.,Tejero, T.,Alexakis, A.,Grosjean, F.,Normant, J.

, p. 255 - 257 (2007/10/02)

Symmetrical vicinal (R*,R*) -d,l-diamines were prepared from the corresponding imines and low valent titanium species generated by the action of titanium tetrachloride on amalgamated magnesium.

REACTIONS OF ALIPHATIC 1,2-DIAMINES WITH 2,2'-DICHLORODIETHYL ETHER

Glinka, Ryszard,Mikiciuk-Olasik, Elzbieta,Kotelko, Barbara,Strzelczyk, Marek

, p. 203 - 212 (2007/10/02)

Studies have been carried out on reations of condensation of aliphatic 1,2-diamines with 2,2'-dichlorodiethyl ether.It has been established that in the case of 1,2-diaminopropane and 2,3-diaminobutane appropriate derivatives of morpholine are formed, while in the case of their N,N'-dialkyl derivatives formation of alkyl substituted octahydro-1,4,7-oxadiazonines takes place.When some amines possessing aromatic substituents (N,N'-dibenzylethylenediamine, N,N'-dimethylstilbenediamine) at α carbon atom are used as substrates, derivatives of imidazoline are formed.

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