1H-Indole-2-carboxylicacid,2,3-dihydro-,methylester,(2R)-(9CI)

Base Information

Chemical Name:1H-Indole-2-carboxylicacid,2,3-dihydro-,methylester,(2R)-(9CI)
CAS No.:293737-30-1
Molecular Formula:C₁₀H₁₁NO₂
Molecular Weight:177.203
Hs Code.:2933998090
Mol file:293737-30-1.mol

Synonyms:1H-Indole-2-carboxylicacid,2,3-dihydro-,methylester,(2R)-(9CI);(R)-2,3-dihydro-1H-indol-2-carboxylic acid Methyl ester

Suppliers and Price of 1H-Indole-2-carboxylicacid,2,3-dihydro-,methylester,(2R)-(9CI)

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

Apolloscientific
Methyl(2r)-2,3-dihydro-1H-indole-2-carboxylate 95%
1g
$ 345.00

Total 2 raw suppliers

Chemical Property of 1H-Indole-2-carboxylicacid,2,3-dihydro-,methylester,(2R)-(9CI)

Chemical Property:

PSA：38.33000
LogP:1.33420

Purity/Quality:

99% ^*data from raw suppliers

Methyl(2r)-2,3-dihydro-1H-indole-2-carboxylate 95% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1H-Indole-2-carboxylicacid,2,3-dihydro-,methylester,(2R)-(9CI)

There total 11 articles about 1H-Indole-2-carboxylicacid,2,3-dihydro-,methylester,(2R)-(9CI) 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: 94.0%

: (R)-1-tosylindoline-2-carboxylic acid methyl ester

(R)-indoline-2-carboxylic acid methyl ester: 293737-30-1
(R)-indoline-2-carboxylic acid methyl ester

Guidance literature:: With methanol; magnesium; at 20 ℃; for 3h; enantioselective reaction;

Reference yield: 92.0%

: 59040-84-5,130791-93-4,141410-06-2
indoline-2-carboxylic acid methyl ester

: 721968-93-0
3-methoxyphenyl allyl carbonate

(R)-indoline-2-carboxylic acid methyl ester: 293737-30-1
(R)-indoline-2-carboxylic acid methyl ester

: 1061617-43-3
methyl (S)-N-(allyloxycarbonyl)indoline-2-carboxylate

Guidance literature:: With immobilized NZL-101 Candida antarctica lipase A; In various solvent(s); at 30 ℃; for 4h;
DOI:10.1016/j.tetasy.2008.06.010

Reference yield: 42.9%

: 59040-84-5,130791-93-4,141410-06-2
indoline-2-carboxylic acid methyl ester

(R)-indoline-2-carboxylic acid methyl ester: 293737-30-1
(R)-indoline-2-carboxylic acid methyl ester

: 141410-06-2
(S)-indoline-2-carboxylic acid methyl ester

Guidance literature:: With sodium hydroxide; Everlase; In water; at 35 ℃; for 3h; pH=7.8 - 8.2; Product distribution / selectivity; Resolution of racemate; Enzymatic reaction;