Methyl camphorate

Base Information

Chemical Name:Methyl camphorate
CAS No.:26252-15-3
Molecular Formula:C₁₁H₁₈O₄
Molecular Weight:214.262
Hs Code.:
UNII:ZG0T7I1N0L,2J40EV4V2Z

Synonyms:Methyl camphorate;Methyl camphorate, (+/-)-;219496-46-5;Methyl camphorate, (-)-;ZG0T7I1N0L;2J40EV4V2Z;Methyl camphorate, (1S,3R)-;(1S,3R)-3-(methoxycarbonyl)-1,2,2-trimethylcyclopentanecarboxylic acid;1,3-Cyclopentanedicarboxylic acid, 1,2,2-trimethyl-, 3-methyl ester, cis-;(1S,3R)-3-(METHOXYCARBONYL)-1,2,2-TRIMETHYLCYCLOPENTANE-1-CARBOXYLIC ACID;1,3-Cyclopentanedicarboxylic acid, 1,2,2-trimethyl-, 3-methyl ester, (1S,3R)-;UNII-ZG0T7I1N0L;26252-15-3;UNII-2J40EV4V2Z;SCHEMBL2533909;VFNNTVXOZWMVGX-WRWORJQWSA-N;METHYL CAMPHORATE [WHO-DD];AKOS000267791;CS-0260586;CS-0356568;EN300-7548007;29606-91-5

Suppliers and Price of Methyl camphorate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 1 raw suppliers

Chemical Property of Methyl camphorate

Chemical Property:

XLogP3:1.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:214.12050905
Heavy Atom Count:15
Complexity:295

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1(C(CCC1(C)C(=O)O)C(=O)OC)C
Isomeric SMILES:C[C@@]1(CC[C@H](C1(C)C)C(=O)OC)C(=O)O

Technology Process of Methyl camphorate

There total 1 articles about Methyl camphorate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 67-56-1
methanol

: 76-32-4
(±)-camphoric acid anhydride

: 26252-15-3,26252-19-7,29606-91-5,29606-95-9,29607-02-1,29722-60-9
(+/-)-3-methyl hydrogen 1,2,2-trimethyl-cis-1,3-cyclopentanedicarboxylate

: 26252-16-4,26252-20-0,29606-94-8,29606-98-2,29606-99-3,29722-59-6
(+/-)-3-methyl hydrogen 2,2,3-trimethyl-cis-1,3-cyclopentanedicarboxylate

Guidance literature:: for 48h; Title compound not separated from byproducts; Heating;
DOI:10.1139/v88-009

Reference yield:

: 64-17-5
ethanol

: 26252-15-3,26252-19-7,29606-91-5,29606-95-9,29607-02-1,29722-60-9
(1R)-trans-camphoric acid-3-methyl ester

: 595-32-4
(1R,3R)-1,2,2-Trimethyl-cyclopentane-1,3-dicarboxylic acid

: 124-83-4
D-(+)-camphoric acid

: 31147-48-5
(1R)-1.2.2-trimethyl-3t-hydroxymethyl-cyclopentane-carboxylic acid-(1r)

: 31147-48-5
(1R)-1.2.2-trimethyl-3c-hydroxymethyl-cyclopentane-carboxylic acid-(1r)

Guidance literature:: DOI:10.1021/ja01850a053

Reference yield:

: 26252-15-3,26252-19-7,29606-91-5,29606-95-9,29607-02-1,29722-60-9
(1R)-trans-camphoric acid-3-methyl ester

: 5333-17-5,6787-29-7,19908-60-2,20536-65-6
(1R)-3t-carbamoyl-2,2,3c-trimethyl-cyclopentane-r-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride / Behandeln einer aether. Loesung des Reaktionsprodukts mit Ammoniak

2: aq.-ethanolic NaOH-solution

With sodium hydroxide; thionyl chloride;