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2-Bromo-3-methoxy-3-methylbutanoic acid is a chemical compound with the molecular formula C7H13BrO3. It is a derivative of butanoic acid, featuring a bromine atom, a methoxy group, and a methyl group attached to the carbon chain. 2-BROMO-3-METHOXY-3-METHYLBUTANOIC ACID is known for its chemical properties and reactivity, making it a valuable building block in various organic molecules and a promising candidate in pharmaceutical research and development.

75974-47-9

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75974-47-9 Usage

Uses

Used in Organic Synthesis:
2-Bromo-3-methoxy-3-methylbutanoic acid is used as a building block in organic synthesis for the creation of various organic molecules. Its unique structure and functional groups contribute to the formation of complex organic compounds, enhancing the diversity of chemical products.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-Bromo-3-methoxy-3-methylbutanoic acid serves as a key intermediate in the development of new drug molecules. Its chemical properties allow for the modification and synthesis of potential therapeutic agents, contributing to the advancement of medicinal chemistry.
Used in the Production of Pharmaceuticals:
2-Bromo-3-methoxy-3-methylbutanoic acid is utilized in the manufacturing process of various pharmaceuticals. Its presence in the synthesis of active pharmaceutical ingredients (APIs) highlights its importance in the development of new medications and treatments.
Used in Agrochemicals Production:
2-BROMO-3-METHOXY-3-METHYLBUTANOIC ACID also finds application in the production of agrochemicals, where it plays a role in the synthesis of pesticides, herbicides, and other agricultural chemicals. Its reactivity and functional groups contribute to the development of effective and targeted agrochemical products.
Used in Medicinal Chemistry for Drug Development:
2-Bromo-3-methoxy-3-methylbutanoic acid has potential applications in the field of medicinal chemistry, where it is employed for the development of new drug molecules. Its unique structure and properties make it a valuable component in the design and synthesis of innovative pharmaceuticals with potential therapeutic benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 75974-47-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,9,7 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 75974-47:
(7*7)+(6*5)+(5*9)+(4*7)+(3*4)+(2*4)+(1*7)=179
179 % 10 = 9
So 75974-47-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H11BrO3/c1-6(2,10-3)4(7)5(8)9/h4H,1-3H3,(H,8,9)

75974-47-9SDS

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 2-BROMO-3-METHOXY-3-METHYLBUTANOIC ACID

1.2 Other means of identification

Product number -
Other names 2-Brom-3-methoxy-3-methyl-buttersaeure

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:75974-47-9 SDS

75974-47-9Relevant academic research and scientific papers

Cyclic peptides

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, (2008/06/13)

To provide a process for the total synthesis of a cyclic peptide, which is useful as antifungal drug, and novel compounds prepared by the synthesis method. A process for synthesizing a cyclic peptide represented by the following formula (I): STR1 wherein X1, X2, X4 and X7 are independently N-methyl-α-amino acid or α-hydroxy acid, provided that at least one of X1, X2, X4 and X7 is a α-hydroxy acid; X3, X6 and X8 are independently α-amino acid; X5 is a cyclic amino acid; X9 is a N-methyl-α-amino acid or α-hydroxy acid substituted by a hydroxy group; and the dotted lines represent intramolecular hydrogen bonds; which process comprises cyclizing a corresponding linear peptide between X5 and X6 via a peptide bond, and a novel compound represented by the formula (I).

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