2737-22-6 Usage
Uses
Used in Flame Retardant Applications:
3-HYDROXY-2,4,6-TRIBROMOBENZALDEHYDE is used as a flame retardant in various industries to reduce the flammability of products such as plastics, textiles, and electronics. Its high thermal stability makes it effective in preventing the spread of fire and enhancing the safety of these materials.
Used in Chemical Production:
3-HYDROXY-2,4,6-TRIBROMOBENZALDEHYDE is also used in the production of other chemicals, contributing to the synthesis of various compounds for different applications.
Used in Plastics Industry:
In the plastics industry, 3-HYDROXY-2,4,6-TRIBROMOBENZALDEHYDE is used as a flame retardant to improve the fire resistance of plastic materials, ensuring they meet safety standards and reducing the risk of fire-related accidents.
Used in Textile Industry:
3-HYDROXY-2,4,6-TRIBROMOBENZALDEHYDE is used in the textile industry to enhance the flame retardancy of fabrics, making them safer for use in applications such as upholstery, curtains, and clothing.
Used in Electronics Industry:
In the electronics industry, 3-HYDROXY-2,4,6-TRIBROMOBENZALDEHYDE is used to reduce the flammability of electronic components and devices, protecting them from potential fire hazards and ensuring the safety of users.
However, due to concerns about the potential toxicity and environmental impact of 3-HYDROXY-2,4,6-TRIBROMOBENZALDEHYDE, there are ongoing efforts to find alternative and safer flame retardant materials to replace it in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 2737-22-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,3 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2737-22:
(6*2)+(5*7)+(4*3)+(3*7)+(2*2)+(1*2)=86
86 % 10 = 6
So 2737-22-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H3Br3O2/c8-4-1-5(9)7(12)6(10)3(4)2-11/h1-2,12H
2737-22-6Relevant academic research and scientific papers
N1,N1-dimethyl-N3-(3-(trifluoromethyl) phenethyl)propane-1,3-diamine, a new lead for the treatment of human African trypanosomiasis
Pham, Ngoc B.,Deydier, Sophie,Labaied, Mehdi,Monnerat, Severine,Stuart, Kenneth,Quinn, Ronald J.
, p. 541 - 551 (2014/03/21)
The natural product, convolutamine I (1), has anti-trypanosomal activity however it has a high molecular weight of 473 due to a presence of 3 bromine atoms. The synthesis of the natural product convolutamine I (1) together with its analogues are presented. A SAR study against Trypanosoma brucei brucei led to compounds with improved physico-chemical properties: lower molecular weight and lower log P while maintaining potency (with a slight 2-fold improvement).
Bromodecarbonylation and bromodecarboxylation of electron-rich benzaldehydes and benzoic acids with oxone and sodium bromide
Koo, Bon-Suk,Kim, Eun-Hoo,Lee, Kee-Jung
, p. 2275 - 2286 (2007/10/03)
Benzaldehydes and benzoic acids bearing ortho- and paraelectron donating substituents having unshared electron-pair have undergone bromodecarbonylation or bromodecarboxylation on treatment with sodium bromide in the presence of Oxone in aqueous methanol.
Asymmetric synthesis of amathamides A and B: Novel alkaloids isolated from Amathia wilsoni
Ramirez Osuna, Moises,Aguirre, Gerardo,Somanathan, Ratnasamy,Molins, Elias
, p. 2261 - 2266 (2007/10/03)
Syntheses of the amathamides A and B ((2S)-N-[(E and Z)-2(2,4-dibromo-5-methoxyphenylethenyl]-1-methyl-2-pyrrolinecarboxamides), new alkaloids isolated from the Tasmanian marine bryozoan Amathia wilsoni, were accomplished by a sequence of reactions starting from 3-hydroxybenzaldehyde.
