1-Phenylpiperidine-4-carbaldehyde

Base Information

Chemical Name:1-Phenylpiperidine-4-carbaldehyde
CAS No.:111153-74-3
Molecular Formula:C12H15NO
Molecular Weight:189.257
Hs Code.:2933399090
DSSTox Substance ID:DTXSID40551081
Wikidata:Q82430595
Mol file:111153-74-3.mol

Synonyms:1-Phenylpiperidine-4-carbaldehyde;111153-74-3;4-formyl-1-phenylpiperidine;1-Phenyl-4-piperidinecarbaldehyde;SCHEMBL1443382;DTXSID40551081;PRQRNNQMKUAVAB-UHFFFAOYSA-N;AKOS006228137;AB24784;DS-3499;SY016536;CS-0440875;O10435;A894778

Suppliers and Price of 1-Phenylpiperidine-4-carbaldehyde

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

Crysdot
1-Phenylpiperidine-4-carbaldehyde 95+%
1g
$ 772.00

Chemenu
1-Phenylpiperidine-4-carbaldehyde 95%
1g
$ 729.00

American Custom Chemicals Corporation
1-PHENYLPIPERIDINE-4-CARBALDEHYDE 95.00%
5G
$ 2152.64

American Custom Chemicals Corporation
1-PHENYLPIPERIDINE-4-CARBALDEHYDE 95.00%
1G
$ 1819.13

American Custom Chemicals Corporation
1-PHENYLPIPERIDINE-4-CARBALDEHYDE 95.00%
10G
$ 3668.57

Alichem
1-Phenylpiperidine-4-carbaldehyde
25g
$ 4971.40

Alichem
1-Phenylpiperidine-4-carbaldehyde
10g
$ 2580.84

Alichem
1-Phenylpiperidine-4-carbaldehyde
5g
$ 1691.75

Total 10 raw suppliers

Chemical Property of 1-Phenylpiperidine-4-carbaldehyde

Chemical Property:

PSA：20.31000
LogP:2.16690
Storage Temp.:Inert atmosphere,Store in freezer, under -20°C
XLogP3:3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:189.115364102
Heavy Atom Count:14
Complexity:179

Purity/Quality:

97% ^*data from raw suppliers

1-Phenylpiperidine-4-carbaldehyde 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CN(CCC1C=O)C2=CC=CC=C2
Uses 1-Phenylpiperidine-4-carbaldehyde is a useful reagent in the preparation of 2-?phenylthiazolidine derivatives used as cardiotonic agents.

Technology Process of 1-Phenylpiperidine-4-carbaldehyde

There total 5 articles about 1-Phenylpiperidine-4-carbaldehyde 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: 90.0%

: 697306-45-9
(1-phenylpiperidin-4-yl)methanol

: 111153-74-3
4-formyl-1-phenylpiperidine

Guidance literature:: With N-(tert-butyl)benzenesulfinimidoyl chloride; 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; at -78 - -60 ℃; for 1h;

Reference yield: 74.93%

: 247022-37-3
ethyl 1-phenylpiperidine-4-carboxylate

: 111153-74-3
4-formyl-1-phenylpiperidine

Guidance literature:: With diisobutylaluminium hydride; In dichloromethane; at -78 ℃; for 1h;

Reference yield:

: 1126-09-6
4-carbethoxypiperidine

: 111153-74-3
4-formyl-1-phenylpiperidine

Guidance literature:: Multi-step reaction with 2 steps

1: bis(tri-t-butylphosphine)palladium⁽⁰⁾; potassium phosphate / 1,2-dimethoxyethane / 16 h / 100 °C

2: diisobutylaluminium hydride / dichloromethane / 1 h / -78 °C

With potassium phosphate; bis(tri-t-butylphosphine)palladium⁽⁰⁾; diisobutylaluminium hydride; In 1,2-dimethoxyethane; dichloromethane;