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4-BROMO-1,3-BENZODIOXOLE is a brominated derivative of benzodioxole with the molecular formula C8H7BrO2. It is a white solid chemical compound known for its high melting point and solubility in organic solvents but not in water. 4-BROMO-1,3-BENZODIOXOLE serves as a versatile intermediate in the synthesis of various organic compounds and pharmaceuticals.

6698-13-1

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6698-13-1 Usage

Uses

Used in Pharmaceutical Industry:
4-BROMO-1,3-BENZODIOXOLE is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of novel drug molecules. Its unique structure allows for the creation of new compounds with potential therapeutic applications.
Used in Organic Compounds Synthesis:
In the field of organic chemistry, 4-BROMO-1,3-BENZODIOXOLE is utilized as a building block for the synthesis of complex organic molecules. Its reactivity and structural features make it a valuable component in the formation of various organic substances.
Used in Fragrance Industry:
4-BROMO-1,3-BENZODIOXOLE is employed as a component in the production of fragrances, where its chemical properties contribute to the creation of unique scents and aromas.
Used in Agrochemicals Production:
4-BROMO-1,3-BENZODIOXOLE also finds application in the agrochemical industry, where it is used as an intermediate in the synthesis of various agrochemical products, potentially enhancing crop protection and yield.
Used in Research and Development:
4-BROMO-1,3-BENZODIOXOLE is utilized in research and development settings for the synthesis of innovative compounds. Its potential applications in the pharmaceutical and chemical industries make it a valuable asset for scientific exploration and advancement.

Check Digit Verification of cas no

The CAS Registry Mumber 6698-13-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,9 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6698-13:
(6*6)+(5*6)+(4*9)+(3*8)+(2*1)+(1*3)=131
131 % 10 = 1
So 6698-13-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H5BrO2/c8-5-2-1-3-6-7(5)10-4-9-6/h1-3H,4H2

6698-13-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Bromo-1,3-benzodioxole

1.2 Other means of identification

Product number -
Other names 4-BROMO-1,3-BENZODIOXOLE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6698-13-1 SDS

6698-13-1Relevant academic research and scientific papers

FUSED RING PYRIMIDINE COMPOUND, INTERMEDIATE, AND PREPARATION METHOD, COMPOSITION AND USE THEREOF

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Paragraph 0386-0388, (2018/08/12)

Disclosed area fused ring pyrimidine compound, and an intermediate, a preparation method, a composition and a use thereof. The fused ring pyrimidine compound is a compound as shown in formula I, a tautomer, an enantiomer, a diastereoisomer, a pharmaceutically acceptable salt, a metabolite, a metabolic precursor or a prodrug thereof, wherein the above-mentioned compound is used for the preparation of a medicine for preventing, remitting or treating one or more of immune system diseases, autoimmune diseases, cell proliferative diseases, allergic disorders and cardiovascular diseases, and the compound has a strong inhibitory effect on the Janues kinase, FGFR kinase, FLT3 kinase and Src family kinase.

Synthesis of ACAT inhibitors through substitution using allylic picolinate and copper reagent

Kobayashi, Yuichi,Lalitnorasate, Paveena,Kaneko, Yuki,Kiyotsuka, Yohei,Endo, Yoshiki

scheme or table, p. 6018 - 6021 (2010/11/21)

Amide of an octanoic acid possessing an aryl group at C3 position is a highly potent ACAT inhibitor. In this paper, we describe a synthetic access to this class of compounds as optically active forms. The key reaction is substitution of the allylic picoli

Synthesis of 5,6-methylenedioxy-1-tetralone. An aryl Grignard approach from guaiacol

Klix, Russell C.,Cain, Michael H.,Bhatia, Ashok V.

, p. 6413 - 6414 (2007/10/02)

A convenient synthesis of 5,6-methylenedioxy-1-tetralone (1) is described. The main features of this synthesis are the formation of 6 via a Grignard reaction using succinic anhydride followed by selective reduction and Friedel-Crafts cyclization to generate the desired tetralone 1.

Phenyl-substituted sulfonamides

-

, (2008/06/13)

Novel N-[pyrimidin-2-yl]- and [triazin-2-yl]-aminocarbonyl]-1,3-benzodioxolesulfonamides and 1,4-benzodioxansulfonamides are useful as plant growth regulants and in particular as herbicides.

Substituted sulfonamides 1,3-benzodioxole

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, (2008/06/13)

Novel N-[pyrimidin-2-yl]- and [triazin-2-yl]aminocarbonyl-1,3-benzodioxolesulfonamides and 1,4-benzodioxansulfonamides are useful as plant growth regulants and in particular as herbicides.

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