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Methyl 1-(bromomethyl)cyclopropanecarboxylate is a cyclopropane derivative with the chemical formula C6H9BrO2. It features a methyl ester and a bromomethyl group, making it a versatile building block in organic synthesis for constructing more complex molecules. Its unique structure and reactivity contribute to its value in creating a broad spectrum of chemical compounds for various applications.

43161-30-4

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43161-30-4 Usage

Uses

Used in Organic Synthesis:
Methyl 1-(bromomethyl)cyclopropanecarboxylate serves as a key building block in organic synthesis, utilized for creating a variety of complex molecules. Its presence of both a methyl ester and a bromomethyl group facilitates multiple reaction pathways, making it a valuable component in the synthesis of diverse chemical entities.
Used in Pharmaceutical Research and Development:
In the pharmaceutical industry, methyl 1-(bromomethyl)cyclopropanecarboxylate is employed in research and development for its potential to contribute to the creation of new drugs. Its unique reactivity and structural features can be harnessed to develop novel therapeutic agents with specific medicinal properties.
Used in Agricultural Chemical Production:
Methyl 1-(bromomethyl)cyclopropanecarboxylate also finds application in the production of agricultural chemicals. Its chemical properties allow it to be incorporated into the development of pesticides, herbicides, and other agrochemicals that are designed to improve crop yields and protect plants from pests and diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 43161-30-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,3,1,6 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 43161-30:
(7*4)+(6*3)+(5*1)+(4*6)+(3*1)+(2*3)+(1*0)=84
84 % 10 = 4
So 43161-30-4 is a valid CAS Registry Number.

43161-30-4SDS

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 methyl 1-(bromomethyl)cyclopropane-1-carboxylate

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:43161-30-4 SDS

43161-30-4Downstream Products

43161-30-4Relevant academic research and scientific papers

DIAMINE DERIVATIVES

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Page/Page column 149, (2008/06/13)

A compound represented by formula (1):Q1-Q2-To-N(R1) -Q3-N(R2)-T1-Q4 [wherein R1 and R2 are hydrogen atoms or the like; Q1 is a saturated or unsaturated, 5- or 6- membered cyclic hydrocarbon group which may be substituted, or the like; Q2 is a single bond or the like; Q3 represents the following group: (wherein Q5 is an alkylene group having 1 to 8 carbon atoms, or the like); and T0 and T1 are carbonyl groups or the like], a salt thereof, a solvate thereof, or an N-oxide thereof. The compound is useful as an agent for preventing and/or treating cerebral infarction, cerebral embolism, myocardial infarction, angina pectoris, pulmonary infarction, pulmonary embolism, Buerger's disease, deep venous thrombosis, disseminated intravascular coagulation syndrome, thrombus formation after artificial valve or joint replacement, thrombus formation and reocclusion after angioplasty, systemic inflammatory response syndrome (SIRS), multiple organ dysfunction syndrome (MODS), thrombus formation during extracorporeal circulation, or blood clotting upon blood drawing.

Diamine derivatives

-

, (2008/06/13)

A compound represented by the general formula (1): Q1-Q2-T0-N(R1)-Q3-N(R2)-T1-Q4??(1) wherein R1 and R2 are hydrogen atoms or the like; Q1 is a saturated or unsaturated, 5- or 6-membered cyclic hydrocarbon group which may be substituted, or the like; Q2 is a single bond or the like; Q3 is a group in which Q5 is an alkylene group having 1 to 8 carbon atoms, or the like; and T0 and T1 are carbonyl groups or the like; a salt thereof, a solvate thereof, or an N-oxide thereof. The compound is useful as an agent for preventing and/or treating cerebral infarction, cerebral embolism, myocardial infarction, angina pectoris, pulmonary infarction, pulmonary embolism, Buerger's disease, deep venous thrombosis, disseminated intravascular coagulation syndrome, thrombus formation after valve or joint replacement, thrombus formation and reocclusion after angioplasty, systemic inflammatory response syndrome (SIRS), multiple organ dysfunction syndrome (MODS), thrombus formation during extracorporeal circulation, or blood clotting upon blood drawing.

DIAMINE DERIVATIVES

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Page 137, (2008/06/13)

A compound represented by the general formula (1):Q1-Q2-T0-N(R1)-Q3-N(R2)-T1-Q4 wherein R1 and R2 are hydrogen atoms or the like; Q1 is a saturated or unsaturated, 5- or 6- membered cyclic hydrocarbon group which may be substituted, or the like; Q2 is a single bond or the like; Q3 is a group in which Q5 is an alkylene group having 1 to 8 carbon atoms, or the like; and T0 and T1 are carbonyl groups or the like; a salt thereof, a solvate thereof, or an N-oxide thereof. The compound is useful as an agent for preventing and/or treating cerebral infarction, cerebral embolism, myocardial infarction, angina pectoris, pulmonary infarction, pulmonary embolism, Buerger's disease, deep venous thrombosis, disseminated intravascular coagulation syndrome, thrombus formation after valve or joint replacement, thrombus formation and reocclusion after angioplasty, systemic inflammatory response syndrome (SIRS), multiple organ dysfunction syndrome (MODS), thrombus formation during extracorporeal circulation, or blood clotting upon blood drawing.

Ethanoarachidonic Acids. A New Class of Arachidonic Acid Cascade Modulators. 2. Polyethano Compounds

Nicolaou, K. C.,Hernandez, P. E.,Ladduwahetty, T.,Randall, J. L.,Webber, S. E.,et al.

, p. 5403 - 5404 (2007/10/02)

The total synthesis and preliminary biological data of di- and triethanoarachidonic acids 1-4 are described.

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