Chroman-4-amine

Base Information

Chemical Name:Chroman-4-amine
CAS No.:188198-38-1
Molecular Formula:C9H11NO
Molecular Weight:149.192
Hs Code.:2932999099
European Community (EC) Number:837-783-0
ChEMBL ID:CHEMBL4563095
DSSTox Substance ID:DTXSID60940312
Nikkaji Number:J2.443.946A
Mol file:188198-38-1.mol

Synonyms:chroman-4-amine

Suppliers and Price of Chroman-4-amine

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

Matrix Scientific
(S)-3,4-Dihydro-2H-chromen-4-aminehydrochloride 97%
1g
$ 756.00

Matrix Scientific
(S)-3,4-Dihydro-2H-chromen-4-aminehydrochloride 97%
5g
$ 2160.00

J&W Pharmlab
(S)-Chroman-4-ylamine 97%
1g
$ 250.00

Crysdot
(S)-Chroman-4-amine 95+%
1g
$ 246.00

Chemenu
(S)-Chroman-4-amine 95%
1g
$ 561.00

Biosynth Carbosynth
(S)-Chroman-4-ylamine
250 mg
$ 200.00

Biosynth Carbosynth
(S)-Chroman-4-ylamine
100 mg
$ 100.00

Biosynth Carbosynth
(S)-Chroman-4-ylamine
50 mg
$ 60.00

Biosynth Carbosynth
(S)-Chroman-4-ylamine
1 g
$ 480.00

Biosynth Carbosynth
(S)-Chroman-4-ylamine
500 mg
$ 300.00

Total 25 raw suppliers

Chemical Property of Chroman-4-amine

Chemical Property:

Vapor Pressure:0.0449mmHg at 25°C
Refractive Index:1.559
Boiling Point:237.4 °C at 760 mmHg
PKA:8.87±0.20(Predicted)
Flash Point:102.1 °C
PSA：35.25000
Density:1.106 g/cm³
LogP:2.16920
Storage Temp.:2-8°C(protect from light)
XLogP3:0.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:149.084063974
Heavy Atom Count:11
Complexity:138

Purity/Quality:

99%, ^*data from raw suppliers

(S)-3,4-Dihydro-2H-chromen-4-aminehydrochloride 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1COC2=CC=CC=C2C1N

Technology Process of Chroman-4-amine

There total 7 articles about Chroman-4-amine 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:

: 491-37-2
2,3-dihydro-4H-1-benzopyran-4-one

: 188198-38-1
(4S)-3,4-dihydro-2H-l-benzopyran-4-amine

Guidance literature:: With D-Glucose; glutamate dehydrogenase; L-alanin; ω-transaminase from Vibrio f luvialis; PLP; nicotinamide adenine dinucleotide; lactate dehydrogenase; In aq. phosphate buffer; at 30 ℃; for 24h; pH=7; enantioselective reaction; Enzymatic reaction;
DOI:10.1021/cs400002d

Reference yield:

: 491-37-2
2,3-dihydro-4H-1-benzopyran-4-one

: 210488-55-4
(R)-chroman-4-ylamine

: 188198-38-1
(4S)-3,4-dihydro-2H-l-benzopyran-4-amine

Guidance literature:: With L-alanin; alanine dehydrogenase; formate dehydrogenase from Candida boidinii; ω-transaminase from variant Arthrobacter citreus; PLP; ammonium formate; nicotinamide adenine dinucleotide; In aq. phosphate buffer; at 30 ℃; for 24h; pH=7; enantioselective reaction; Enzymatic reaction;
DOI:10.1021/cs400002d