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1-Methylcycloheptanecarboxylic acid methyl ester is an organic compound with the molecular formula C10H18O2. It is a derivative of cycloheptane, a seven-membered cyclic hydrocarbon, with a methyl group attached to the first carbon atom and a carboxylic acid group at the seventh carbon atom. The carboxylic acid group is further esterified with a methyl group, resulting in the formation of a methyl ester. 1-Methylcycloheptanecarboxylic acid methyl ester is characterized by its unique structure, which provides it with specific chemical properties and potential applications in various fields, such as pharmaceuticals and chemical synthesis. It is a colorless liquid with a distinct odor and is insoluble in water but soluble in organic solvents. The compound can be synthesized through various chemical reactions, such as the esterification of 1-methylcycloheptanecarboxylic acid with methanol in the presence of an acid catalyst.

7362-77-8

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7362-77-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7362-77-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,6 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7362-77:
(6*7)+(5*3)+(4*6)+(3*2)+(2*7)+(1*7)=108
108 % 10 = 8
So 7362-77-8 is a valid CAS Registry Number.

7362-77-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 1-methylcycloheptane-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:7362-77-8 SDS

7362-77-8Relevant academic research and scientific papers

Nickel-catalyzed direct arylation of C(sp3)-H bonds in aliphatic amides via bidentate-chelation assistance

Aihara, Yoshinori,Chatani, Naoto

supporting information, p. 898 - 901 (2014/02/14)

The Ni-catalyzed, direct arylation of C(sp3)-H (methyl and methylene) bonds in aliphatic amides containing an 8-aminoquinoline moiety as a bidentate directing group with aryl halides is described. Deuterium-labeling experiments indicate that the C-H bond cleavage step is fast and reversible. Various nickel complexes including both Ni(II) and Ni(0) show a high catalytic activity. The results of a series of mechanistic experiments indicate that the catalytic reaction does not proceed through a Ni(0)/Ni(II) catalytic cycle, but probably through a Ni(II)/Ni(IV) catalytic cycle.

Nickel-catalyzed site-selective alkylation of unactivated C(sp 3)-H bonds

Wu, Xuesong,Zhao, Yan,Ge, Haibo

supporting information, p. 1789 - 1792 (2014/03/21)

The direct alkylation of unactivated sp3 C-H bonds of aliphatic amides was achieved via nickel catalysis with the assist of a bidentate directing group. The reaction favors the C-H bonds of methyl groups over the methylene C-H bonds and tolerates various functional groups. Moreover, this reaction shows a predominant preference for sp3 C-H bonds of methyl groups via a five-membered ring intermediate over the sp2 C-H bonds of arenes in the cyclometalation step.

Copper-catalyzed site-selective intramolecular amidation of unactivated C(sp3)-H bonds

Wu, Xuesong,Zhao, Yan,Zhang, Guangwu,Ge, Haibo

supporting information, p. 3706 - 3710 (2014/04/17)

The intramolecular dehydrogenative amidation of aliphatic amides, directed by a bidentate ligand, was developed using a copper-catalyzed sp3 C-H bond functionalization process. The reaction favors predominantly the C-H bonds of β-methyl groups over the unactivated methylene C-H bonds. Moreover, a preference for activating sp3 C-H bonds of β-methyl groups, via a five-membered ring intermediate, over the aromatic sp2 C-H bonds was also observed in the cyclometalation step. Additionally, sp3 C-H bonds of unactivated secondary sp3 C-H bonds could be functionalized by favoring the ring carbon atoms over the linear carbon atoms. Getting ahead on tams: The intramolecular dehydrogenative amidation of aliphatic amides, directed by a bidentate ligand, was developed using a copper-catalyzed sp 3 C-H bond functionalization process to deliver β-lactams. The reaction favors the C-H bonds of β-methyl groups over the unactivated methylene C-H bonds, as well as aromatic C(sp2)-H bonds and unactivated secondary C(sp3)-H bonds of rings.

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