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"N^(1),N^(2)-bis(2-bromobenzyl)-N^(1),N^(2)-dimethylpropane-1,3-diamine" is a complex organic compound with the molecular formula C17H22Br2N2. It is a derivative of propane-1,3-diamine, where two of the hydrogen atoms are replaced by 2-bromobenzyl groups, and the remaining two nitrogen atoms are each substituted with a methyl group. N(1),N(2)-bis(2-bromobenzyl)-N(1),N(2)-dimethylpropane-1,3-diamine is characterized by its symmetrical structure, with two bromine atoms attached to the benzyl groups, which are in turn connected to the central propane-1,3-diamine backbone. The presence of bromine atoms makes it a potential candidate for use in the synthesis of various pharmaceuticals and agrochemicals, as well as in the production of dyes and other specialty chemicals. Its specific applications may include acting as an intermediate in the synthesis of more complex molecules or as a reagent in organic reactions.

7375-70-4

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7375-70-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7375-70-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,7 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7375-70:
(6*7)+(5*3)+(4*7)+(3*5)+(2*7)+(1*0)=114
114 % 10 = 4
So 7375-70-4 is a valid CAS Registry Number.

7375-70-4Relevant academic research and scientific papers

An amine template strategy to construct successive C-C bonds: Synthesis of benzo[: H] quinolines by a deaminative ring contraction cascade

McFadden, Timothy Patrick,Nwachukwu, Chideraa Iheanyi,Roberts, Andrew George

supporting information, p. 1379 - 1385 (2022/03/01)

We developed a convergent strategy to build, cyclize and excise nitrogen from tertiary amines for the synthesis of polyheterocyclic aromatics. Biaryl-linked azepine intermediates can undergo a deaminative ring contraction cascade reaction, excising nitrogen with the formation of an aromatic core. This strategy and deaminative ring contraction reaction are useful for the synthesis of benzo[h]quinolines. This journal is

Hypervalent organoantimony compounds 12-ethynyl-tetrahydrodibenz[c,f][1,5]azastibocines: Highly efficient new transmetallating agent for organic halides

Kakusawa, Naoki,Tobiyasu, Yoshinori,Yasuike, Shuji,Yamaguchi, Kentaro,Seki, Hiroko,Kurita, Jyoji

, p. 2953 - 2968 (2007/10/03)

Extremely efficient and high-speed ethynylation of acyl chlorides, aryl iodides and bromides was demonstrated by palladium-catalyzed cross-coupling reaction of N-t-butyl-Sb-ethynyl-5,6,7,12-tetrahydrodibenz[c,f][1,5]azastibocine under mild conditions. Optimization and generalization of the hypervalent antimony-mediated coupling reaction are presented in detail. Single-crystal X-ray analysis of the N-methyl-1,5-azastibocine revealed that the remarkable reactivity enhancement of the azastibocine was derived from elongation of the antimony-ethynyl carbon bond originated from Sb-N intramolecular non-bonding interaction.

TRANSANNULAR BOND FORMATION BETWEEN THE ANTIMONY AND THE NITROGEN ATOMS IN DIBENZAZASTIBOCINE SYSTEM. FORMATION OF X-Sb-X AND X-Sb-N(1+) HYPERVALENT BOND

Ohkata, Katsuo,Ohnishi, Masako,Akiba, Kin-ya

, p. 5401 - 5404 (2007/10/02)

6-Methyl-5,6,7,12-tetrahydro-12-p-tolyldibenzazastibocine (1) was prepared by means of one-pot reaction of di(o-bromobenzyl)methylamine (2), butyllithium, and antimony trichloride, followed by p-tolyllithium in 23percent yield.Halogenation of 1

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