Welcome to LookChem.com Sign In|Join Free
  • or
3,4-DIBROMO-2-NITROTHIOPHENE, with the chemical formula C4H2Br2NO2S, is a yellow solid that belongs to the class of nitrothiophenes. It is characterized by its high reactivity and strong electron-withdrawing properties, which make it a valuable intermediate in the synthesis of various chemical compounds. 3,4-DIBROMO-2-NITROTHIOPHENE is utilized in the production of pharmaceuticals and agrochemicals, and its unique structure contributes to its diverse research and industrial applications. However, due to its potential toxicity and environmental impact, it is essential to adhere to proper handling and disposal guidelines when working with 3,4-DIBROMO-2-NITROTHIOPHENE.

35633-91-1

Post Buying Request

35633-91-1 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

35633-91-1 Usage

Uses

Used in Pharmaceutical Industry:
3,4-DIBROMO-2-NITROTHIOPHENE is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its reactivity and electron-withdrawing properties enable the development of new drugs with improved therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, 3,4-DIBROMO-2-NITROTHIOPHENE serves as a crucial component in the production of pesticides and other agrochemicals. Its unique structure and reactivity contribute to the creation of effective and targeted pest control solutions.
Used in Chemical Research:
3,4-DIBROMO-2-NITROTHIOPHENE is utilized as a research compound in various scientific studies. Its properties make it an interesting subject for exploring new chemical reactions, synthesis methods, and potential applications in different fields.
Used in Industrial Applications:
Due to its versatility and reactivity, 3,4-DIBROMO-2-NITROTHIOPHENE is employed in various industrial applications, including the synthesis of dyes, plastics, and other specialty chemicals. Its electron-withdrawing properties and unique structure make it a valuable component in the development of innovative materials and products.

Check Digit Verification of cas no

The CAS Registry Mumber 35633-91-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,6,3 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 35633-91:
(7*3)+(6*5)+(5*6)+(4*3)+(3*3)+(2*9)+(1*1)=121
121 % 10 = 1
So 35633-91-1 is a valid CAS Registry Number.

35633-91-1Upstream product

35633-91-1Relevant academic research and scientific papers

Towards novel thieno-fused subporphyrazines via functionalized thiophene precursors

Rasmussen, Mads Georg,Gotfredsen, Henrik,Kadziola, Anders,Nielsen, Mogens Br?ndsted

supporting information, p. 357 - 368 (2020/04/28)

Thieno-fused subporphyrazines (TPs) containing a central and axially substituted boron atom are a class of compounds with interesting optical and redox properties. Here we present our efforts towards expanding this class of compounds using various thiophene substrates that were prepared by cyanation or nitration of 3,4-dibromothiophene. Moreover, we show that one TP derivative forms a 2:1 complex in the solid state with C70.

Heterocyclic-ring condensed benzothiazine compound

-

, (2008/06/13)

The invention provides a novel heterocyclic ring condensed benzothiazine compound which is effective for prevention or remedy of disease, in which histamine, leukotriene and the like participate. The heterocyclic ring condensed benzothiazine compound of the present invention or a pharmacologically acceptable salt thereof is effective for prevention or remedy of disease, in which a chemical mediator, such as histamine, leukotriene and the like, participate, for example, asthma, allergic coryza, atopic dermatitis, hives, hay fever, gastrointestinal allergy, food allergy and the like. Further, the heterocyclic ring condensed benzothiazine compound of the present invention, its pharmacologically acceptable salt or hydrates thereof is represented by the following formula: In the formula, the ring Het represents an unsaturated heterocyclic ring; R1and R2are the same as or different from each other, and each represents halogen atom, a lower alkyl group that may be substituted with a halogen atom, a lower alkoxy group that may be substituted with a halogen atom, a lower alkyl lower alkoxy group, cyano group; D represents a lower alkylene group and the like that may have a substituent; Q represents, for example, the formula —NR20R2(in the formula, R20and R21are the same as or different from each other, and each represents hydrogen atom, a lower alkyl group that may be substituted with a halogen atom, an aryl group that may have a substituent, an arylalkyl group that may have a substituent, a heteroaryl group that may have a substituent or a heteroarylalkyl group that may have a substituent, or R20and R21may form a 3- to 8-membered ring along with the nitrogen atom to which they are bound); and x represents an integer of from 1 to 2.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 35633-91-1