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Methyl 3-oxocycloheptanecarboxylate is a synthetic organic compound with a chemical formula C9H14O3. It is a clear, colorless liquid with a fruity odor and is commonly used as a flavoring agent in the fragrance and food industries. This chemical is a derivative of cycloheptanecarboxylic acid and is commonly used in the synthesis of various pharmaceuticals and agrochemicals. It is known for its ability to impart a fruity and sweet aroma and taste, and is often used in the production of perfumes, soaps, and other scented products. However, it should be handled with care as it can be irritating to the skin, eyes, and respiratory system.

37746-13-7

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37746-13-7 Usage

Uses

Used in Flavor and Fragrance Industry:
Methyl 3-oxocycloheptanecarboxylate is used as a flavoring agent for its fruity and sweet aroma and taste, making it suitable for use in the production of perfumes, soaps, and other scented products.
Used in Pharmaceutical and Agrochemical Industries:
Methyl 3-oxocycloheptanecarboxylate is used as a synthetic intermediate in the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new drugs and agricultural products.

Check Digit Verification of cas no

The CAS Registry Mumber 37746-13-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,7,4 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 37746-13:
(7*3)+(6*7)+(5*7)+(4*4)+(3*6)+(2*1)+(1*3)=137
137 % 10 = 7
So 37746-13-7 is a valid CAS Registry Number.

37746-13-7SDS

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 3-oxocycloheptane-1-carboxylate

1.2 Other means of identification

Product number -
Other names Cycloheptanecarboxylic acid,3-oxo-,methyl ester

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:37746-13-7 SDS

37746-13-7Downstream Products

37746-13-7Relevant academic research and scientific papers

Organic dye-catalyzed radical ring expansion reaction

Deguchi, Masato,Fujiya, Akitoshi,Yamaguchi, Eiji,Tada, Norihiro,Uno, Bunji,Itoh, Akichika

, p. 15825 - 15830 (2018/05/04)

Herein, we reported an attractive method for synthesizing medium-sized rings that are catalyzed by erythrosine B under fluorescent light irradiation. This synthetic approach featured mild conditions, a facile procedure, a broad substrate scope, and modera

Combined effects on selectivity in Fe-catalyzed methylene oxidation

Chen, Mark S.,White, M. Christina

scheme or table, p. 533 - 571 (2010/10/05)

Methylene C-H bonds are among the most difficult chemical bonds to selectively functionalize because of their abundance in organic structures and inertness to most chemical reagents. Their selective oxidations in biosynthetic pathways underscore the power of such reactions for streamlining the synthesis of molecules with complex oxygenation patterns. We report that an iron catalyst can achieve methylene C-H bond oxidations in diverse natural-product settings with predictable and high chemo-, site-, and even diastereoselectivities. Electronic, steric, and stereoelectronic factors, which individually promote selectivity with this catalyst, are demonstrated to be powerful control elements when operating in combination in complex molecules. This small-molecule catalyst displays site selectivities complementary to those attained through enzymatic catalysis.

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