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1-bromo-4-(3-methylbut-3-enyloxy)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1254733-86-2

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1254733-86-2 Usage

Category

bromobenzene derivatives the compound belongs to a group of chemical substances derived from bromobenzene, which is a brominated version of benzene.

Usage

organic synthesis and pharmaceutical research the compound is commonly used as a reactant or building block in the synthesis of more complex organic molecules, as well as in the development and study of pharmaceutical drugs.

Structure

benzene ring with a bromine atom at position 1 the compound features a benzene ring, which is a six-carbon ring with alternating single and double bonds, and a bromine atom attached to the first carbon atom of the ring.

Structure

3-methylbut-3-enyloxy group at position 4 the compound also has a 3-methylbut-3-enyloxy group (a butyl group with a double bond and a methyl group attached to the third carbon, and an ether functional group at the end) attached to the fourth carbon atom of the benzene ring.

Physical appearance

colorless to pale yellow liquid the compound is a liquid with a color ranging from colorless to pale yellow.

Odor

strong, pungent the compound has a strong and pungent smell, which can be irritating or unpleasant.

Flammability

flammable the compound can easily catch fire or ignite, and precautions should be taken to prevent fire hazards.

Reactivity

reactive with oxidizing agents the compound can undergo chemical reactions with substances that act as oxidizing agents, which can lead to hazardous situations.

Applications

intermediate in the production of pharmaceuticals, agrochemicals, and other organic compounds the compound is used as a precursor or intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds, making it an important building block in these industries.

Handling precautions

should be handled with care due to its hazardous properties the compound's flammable and reactive nature requires proper handling and storage procedures to ensure safety and prevent accidents.

Check Digit Verification of cas no

The CAS Registry Mumber 1254733-86-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,4,7,3 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1254733-86:
(9*1)+(8*2)+(7*5)+(6*4)+(5*7)+(4*3)+(3*3)+(2*8)+(1*6)=162
162 % 10 = 2
So 1254733-86-2 is a valid CAS Registry Number.

1254733-86-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-bromophenyl 3-methylbut-3-en-1-yl ether

1.2 Other means of identification

Product number -
Other names -

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:1254733-86-2 SDS

1254733-86-2Relevant academic research and scientific papers

SPIRO ISOXAZOLINE COMPOUNDS AS SSTR5 ANTAGONISTS

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Page/Page column 69, (2011/12/04)

Substituted spirocyclic amines of structural formula (I) are selective antagonists of the somatostatin subtype receptor 5 (SSTR5) and are useful for the treatment, control or prevention of disorders responsive to antagonism of SSTR5, such as Type 2 diabetes, insulin resistance, lipid disorders, obesity, atherosclerosis, Metabolic Syndrome, depression, and anxiety.

SUBSTITUTED SPIROCYCLIC AMINES USEFUL AS ANTIDIABETIC COMPOUNDS

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Page/Page column 54, (2010/11/18)

Substituted spirocyclic amines of structural formula I are selective antagonists of the somatostatin subtype receptor 5 (SSTR5) and are useful for the treatment, control or prevention of disorders responsive to antagonism of SSTR5, such as Type 2 diabetes, insulin resistance, lipid disorders, obesity, atherosclerosis, metabolic syndrome, depression, and anxiety.

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