36323-28-1 Usage
Uses
Used in Plastics Industry:
ALPHA,ALPHA,ALPHA',ALPHA'-TETRABROMO-M-XYLENE is used as a flame retardant in the production of plastics to enhance their fire resistance and slow down the spread of fire.
Used in Textile Industry:
In the textile industry, ALPHA,ALPHA,ALPHA',ALPHA'-TETRABROMO-M-XYLENE is utilized as a flame retardant to improve the fire safety of fabrics, particularly those used in upholstery, carpets, and clothing.
Used in Electronic Devices Industry:
ALPHA,ALPHA,ALPHA',ALPHA'-TETRABROMO-M-XYLENE is employed as a flame retardant in the manufacturing of electronic devices to reduce the risk of fire and protect sensitive components from damage due to overheating.
It is important to handle ALPHA,ALPHA,ALPHA',ALPHA'-TETRABROMO-M-XYLENE with caution due to its potential health hazards, such as respiratory and skin irritation. Adhering to safety guidelines and proper handling protocols is crucial when working with this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 36323-28-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,3,2 and 3 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 36323-28:
(7*3)+(6*6)+(5*3)+(4*2)+(3*3)+(2*2)+(1*8)=101
101 % 10 = 1
So 36323-28-1 is a valid CAS Registry Number.
36323-28-1Relevant academic research and scientific papers
Photothermal Side-Chain Bromination of Methyl-, Dimethyl-, and Trimethylbenzenes with N-Bromosuccinimide
Mataka, Shuntaro,Liu, Guo-Bin,Sawada, Tsuyoshi,Kurisu, Masayoshi,Tashiro, Masashi
, p. 1113 - 1119 (2007/10/02)
Tri- and dibromination of methyl-, dimethyl-, and trimethylbenzenes with N-bromosuccinimide were accomplished by photothermal reaction with a tungsten lamp in carbon tetrachloride or benzene. (Dibromomethyl)arenes and (tribromomethyl) derivatives were produced depending upon a solvent used and a substituent on the benzene ring.In the bromination of methylbenzenes without a substituent on the ortho-position, (tribromomethyl)benzenes were formed.On the other hand, ortho-substituted methylbenzenes gave (dibromomethyl)benzenes. α,β-Dibromo-1,2-diarylstilbenes were formed via the debrominative carbon-carbon coupling reaction of ...
REACTION OF THIONYL BROMIDE WITH AROMATIC ALDEHYDES
Saraf, S. D.
, p. 7 - 14 (2007/10/02)
Reaction of thionyl bromide with aromatic aldehydes resulted in the conversion of CHO group into CHBr2.Tolualdehyde gave the corresponding bromomethylbenzal bromides, whereas anisladehyde afforded p-anisic acid as the sole product.
