1-FORMYLINDOLINE

Base Information

Chemical Name:1-FORMYLINDOLINE
CAS No.:2861-59-8
Molecular Formula:C9H9 N O
Molecular Weight:147.177
Hs Code.:2933990090
Mol file:2861-59-8.mol

Synonyms:1-Indolinecarboxaldehyde(6CI,7CI,8CI); 2,3-Dihydroindole-1-carboxaldehyde; N-Formylindoline

Suppliers and Price of 1-FORMYLINDOLINE

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

TRC
N-Formylindoline
100 mg
$ 405.00

SynChem
1-FORMYLINDOLINE 95%
1 g
$ 250.00

Crysdot
Indoline-1-carbaldehyde 95+%
250mg
$ 240.00

Crysdot
Indoline-1-carbaldehyde 95+%
1g
$ 600.00

Crysdot
Indoline-1-carbaldehyde 95+%
5g
$ 1800.00

Chemenu
indoline-1-carbaldehyde 95%
5g
$ 1683.00

Chemenu
indoline-1-carbaldehyde 95%
1g
$ 561.00

Chemcia Scientific
2,3-Dihydro-indole-1-carbaldehyde ＞97%
1 G
$ 270.00

Chemcia Scientific
2,3-Dihydro-indole-1-carbaldehyde ＞97%
0.25 G
$ 120.00

American Custom Chemicals Corporation
1-FORMYLINDOLINE 95.00%
250MG
$ 1593.90

Total 14 raw suppliers

Chemical Property of 1-FORMYLINDOLINE

Chemical Property:

Vapor Pressure:0.00212mmHg at 25°C
Melting Point:63-65°C
Refractive Index:1.681
Boiling Point:165°C 8mm
PKA:1.12±0.20(Predicted)
Flash Point:136.5°C
PSA：20.31000
Density:1.266g/cm³
LogP:1.90640
Solubility.:Dichloromethane, Ethyl Acetate, Methanol

Purity/Quality:

97% ^*data from raw suppliers

N-Formylindoline ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Safety Statements: 22-24/25

MSDS Files:: SDS file from LookChem

Useful:

Uses Indoline metabolite

Technology Process of 1-FORMYLINDOLINE

There total 4 articles about 1-FORMYLINDOLINE 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: 37.0%

: 120-72-9
indole

: 496-15-1
1-indoline

: 2861-59-8
N-formylindoline

Guidance literature:: With formic acid; palladium on activated charcoal; at 70 ℃; for 0.5h;
DOI:10.1055/s-1982-29946

Reference yield:

: 120-72-9
indole

: 64-18-6
formic acid

: 496-15-1
1-indoline

: 2861-59-8
N-formylindoline

Guidance literature:: With palladium 10% on activated carbon; In isopropyl alcohol; at 80 ℃; for 0.5h;
DOI:10.1055/s-0030-1259978

Reference yield:

: 511302-92-4
1-(2-bromoethyl)-2-isocyanatobenzene

: 2861-59-8
N-formylindoline

: 553-03-7
3,4-dihydro-2(1H)-quinolone

: 40411-25-4
2-ethylphenyl isocyanate

: 1-(2,3-dihydroindol-1-yl)-3,4-dihydro-1H-quinolin-2-one

Guidance literature:: With tri-n-butyl-tin hydride; In benzene; at 30 ℃; for 3h; Title compound not separated from byproducts; Photolysis;
DOI:10.1021/jo034002o