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2-METHYLPENTANOIC ANHYDRIDE is a chemical compound with the molecular formula C7H12O3. It is an anhydride derivative of 2-methylpentanoic acid and is commonly used as a reagent in organic synthesis and in the production of pharmaceuticals. 2-METHYLPENTANOIC ANHYDRIDE is a colorless liquid with a pungent odor and is highly reactive, particularly in the presence of moisture. It is flammable and may cause irritation to the skin, eyes, and respiratory system upon exposure.

63169-61-9

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63169-61-9 Usage

Uses

Used in Chemical Production:
2-METHYLPENTANOIC ANHYDRIDE is used as a precursor in the production of various chemicals for its highly reactive nature.
Used in Pharmaceutical Industry:
2-METHYLPENTANOIC ANHYDRIDE is used as a reagent in organic synthesis for the production of pharmaceuticals, contributing to the development of new medications.

Check Digit Verification of cas no

The CAS Registry Mumber 63169-61-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,1,6 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 63169-61:
(7*6)+(6*3)+(5*1)+(4*6)+(3*9)+(2*6)+(1*1)=129
129 % 10 = 9
So 63169-61-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H22O3/c1-5-7-9(3)11(13)15-12(14)10(4)8-6-2/h9-10H,5-8H2,1-4H3

63169-61-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methylpentanoyl 2-methylpentanoate

1.2 Other means of identification

Product number -
Other names 2-methylpentanoic anhydride

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:63169-61-9 SDS

63169-61-9Relevant academic research and scientific papers

PROCESSES FOR PREPARING 4-METHYL-5-NONANONE AND 4-METHYL-5-NONANOL

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Paragraph 0112-0115; 0123-0126, (2020/07/14)

The present invention provides a process for preparing 4-methyl-5-nonanone of the following formula (3): the process comprising at least a step of subjecting 2-methylpentanoic anhydride of the following formula (1) and an n-butyl nucleophilic reagent of the following general formula (2) in which M represents Li, MgZ1, or ZnZ1, wherein Z1 represents a halogen atom or an n-butyl group, to a nucleophilic substitution. reaction Coproduce 4-methyl-5-nonanone (3), as well as a process for preparing 4-methyl-5-nonanol of the following formula (5), the process comprising at least steps of preparing 4-methyl-5-nonanone; and subjecting the obtained 4-methyl-5-nonanone and a reducing agent to a reduction reaction to produce 4-methyl-5-nonanol (5).

NOVEL SULFONIMIDOYLPURINONE COMPOUNDS AND DERIVATIVES FOR THE TREATMENT AND PROPHYLAXIS OF VIRUS INFECTION

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Page/Page column 184; 185, (2016/12/01)

The present invention relates to compounds of formula (I), wherein R 1, R2 and R3 are as described herein, and their prodrugs or pharmaceutically acceptable salt, enantiomer or diastereomer thereof, and compositions including the compounds and methods of using the compounds.

Friedel-Crafts Reaction of 2-Methylfuran with Saturated and α,β-Unsaturated Acid Anhydrides

Scholz, Stefan,Marschall-Weyerstahl, Helga,Weyerstahl, Peter

, p. 1935 - 1950 (2007/10/02)

2-Methylfuran (5) reacts with the saturated acid anhydrides 16 - 26 in the presence of SnCl4 to give the 2-acyl-5-methylfurans 37 - 47 selectively.The unsaturated anhydrides 27 - 32, however, yield mixtures which only in the case of senecioic acid anhydride (29) contain the respective primary product 48.Subsequent reactions lead to the addition products 55 (from 27) and 56 (from 29), and to (E,Z)-mixtures of their enol esters 57 - 62 which could partially be separated and assigned. - The olfactory properties of 2, 37 - 48, 50, 52, and 53 were investigated.

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