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Propan-2-yl 2-methylpentanoate, also known as 2-methyl-2-pentyl pentanoate, is an organic ester compound with the molecular formula C10H20O2. It is formed by the esterification of 2-methylpentanoic acid and propan-2-ol (also known as isopropanol). This colorless liquid has a fruity odor and is commonly used as a flavoring agent in the food and beverage industry, particularly in the production of artificial fruit flavors. Propan-2-yl 2-methylpentanoate is also found in various natural sources, such as fruits and essential oils, contributing to their characteristic aromas. Due to its relatively low toxicity and stable chemical properties, it is considered safe for use in food products within regulated limits.

6639-15-2

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6639-15-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6639-15-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,3 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6639-15:
(6*6)+(5*6)+(4*3)+(3*9)+(2*1)+(1*5)=112
112 % 10 = 2
So 6639-15-2 is a valid CAS Registry Number.

6639-15-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-propyl 2-methylpentanoate

1.2 Other means of identification

Product number -
Other names a-Methyl-tryptophan Methyl Este

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:6639-15-2 SDS

6639-15-2Downstream Products

6639-15-2Relevant academic research and scientific papers

The first examples of selective carbonylation of n-butane and n-pentane

Akhrem, Irena,Orlinkov, Alexander,Afanas'eva, Lyudmila,Petrovskii, Pavel,Vitt, Sergei

, p. 5897 - 5900 (2007/10/03)

The polyhalomethane based superelectrophilic systems allowed us to accomplish the first efficient and selective carbonylation of n-butane and n- pentane with CO. Depending on the nature of the superelectrophilic system, Me3CCOOR or EtCH(Me)COOR (R = H, Alk) can be obtained at -20°C, 1 atm from n-butane and CO after water (α alcohol) treatment in = 90% yield based on the superelectrophilic system. Pentane reacts with CO in the presence d the CBr4 · 2AlBr3 superacid to give a single product, EtC(Me)2COOR, in almost quantitative yield.

ACTIVATION OF MIXED CARBOXILIC α-BROMOTOLUOYL ANHYDRIDES BY SILVER TETRAFLUOROBORATE. SYNTHESIS OF ESTERS AND THIOL ESTERS

Fukuoka, Satoshi,Takimoto, Seiji,Katsuki, Tsutomu,Yamaguchi, Masaru

, p. 4711 - 4712 (2007/10/02)

Mixed carboxylic α-bromotoluoyl anhydrides were activated by silver tetrafluoroborate through intramolecular cyclization and reacted with alcohols or thiols giving the corresponding esters or thiol esters in good yields with the elimination of phtalide.

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