50739-76-9 Usage
Description
2-AMINO-3,5-DIBROMOBENZYL ALCOHOL is an organic compound with the molecular formula C7H7Br2NO. It is a white to off-white solid and is characterized by its unique chemical structure, which includes an amino group, two bromine atoms, and a benzyl alcohol moiety. 2-AMINO-3,5-DIBROMOBENZYL ALCOHOL is synthesized as a byproduct in the production of Ambroxol and Bromhexine, indicating its potential utility in the pharmaceutical industry.
Uses
Used in Pharmaceutical Industry:
2-AMINO-3,5-DIBROMOBENZYL ALCOHOL is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique chemical structure allows it to be a valuable building block for the development of new drugs with potential therapeutic applications.
Used in Chemical Research:
As a byproduct of Ambroxol and Bromhexine synthesis, 2-AMINO-3,5-DIBROMOBENZYL ALCOHOL can be utilized in chemical research to explore its properties and potential reactions. This may lead to the discovery of new compounds or applications in various fields, including materials science, pharmaceuticals, and agrochemicals.
Used in Quality Control and Analysis:
The presence of 2-AMINO-3,5-DIBROMOBENZYL ALCOHOL as an impurity in the synthesis of Bromhexine highlights its importance in quality control and analysis. It can be used as a reference compound to monitor the purity and efficiency of the synthesis process, ensuring the production of high-quality pharmaceutical products.
Check Digit Verification of cas no
The CAS Registry Mumber 50739-76-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,7,3 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 50739-76:
(7*5)+(6*0)+(5*7)+(4*3)+(3*9)+(2*7)+(1*6)=129
129 % 10 = 9
So 50739-76-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H7Br2NO/c8-5-1-4(3-11)7(10)6(9)2-5/h1-2,11H,3,10H2
50739-76-9Relevant articles and documents
Efficient production method of bromhexine hydrochloride
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Paragraph 0081-0087; 0099-0102; 0110-0113; 0121-0123, (2021/01/28)
The invention belongs to the technical field of biological medicines, and particularly relates to an efficient production method of bromhexine hydrochloride. The production method of bromhexine hydrochloride comprises the following steps: (1) reducing 3,5-dibromo-2-aminobenzaldehyde by a reducing agent to obtain an intermediate 3,5-dibromo-2-aminobenzyl alcohol; (2) reacting the intermediate 3,5-dibromo-2-aminobenzyl alcohol with N-methylcyclohexylamine, and then carrying out salt forming reaction to obtain a bromhexine hydrochloride crude product; and (3) purifying the bromhexine hydrochloride crude product to obtain the bromhexine hydrochloride.
A preparation method of bromhexine hydrochloride (by machine translation)
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, (2019/04/10)
The invention belongs to the field of organic synthesis, provides a bromhexine hydrochloride of the preparation method. The invention relates to 2 - aminobenzoic acid ester compound as a raw material, by the bromo reaction, reduction reaction, condensatio
Sunlight-Driven Forging of Amide/Ester Bonds from Three Independent Components: An Approach to Carbamates
Zhao, Yating,Huang, Binbin,Yang, Chao,Chen, Qingqing,Xia, Wujiong
supporting information, p. 5572 - 5575 (2016/11/17)
A photoredox catalytic route to carbamates enabled by visible irradiation (or simply sunlight) has been developed. This process leads to a novel approach to the construction of heterocyclic rings wherein the amide or ester motifs of carbamates were assembled from three isolated components. Large-scale experiments were realized by employing continuous flow techniques, and reuse of photocatalyst demonstrated the green and sustainable aspects of this method.
