2-Phenylcyclopropane-1-carbaldehyde

Base Information

Chemical Name:2-Phenylcyclopropane-1-carbaldehyde
CAS No.:67074-44-6
Molecular Formula:C10H10O
Molecular Weight:146.189
Hs Code.:2912299000
DSSTox Substance ID:DTXSID70400311
Nikkaji Number:J1.057.658J

Synonyms:67074-44-6;2-phenylcyclopropane-1-carbaldehyde;2-PHENYLCYCLOPROPANECARBALDEHYDE;2-Phenyl-Cyclopropanecarbaldehyde;2-Phenylcyclopropanecarboxaldehyde;SCHEMBL446481;2-phenyl-cyclopropanecarbaldehyd;DTXSID70400311;TYJRXMZXDBSURR-UHFFFAOYSA-N;2-phenylcyclopropane-carboxaldehyde;AKOS006282359;EN300-99276;F52095;F8880-8550

Suppliers and Price of 2-Phenylcyclopropane-1-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

Sigma-Aldrich
2-PHENYLCYCLOPROPANECARBALDEHYDE Aldrich
10mg
$ 106.00

Crysdot
2-Phenylcyclopropanecarbaldehyde 95+%
1g
$ 537.00

Chemenu
2-phenylcyclopropane-1-carbaldehyde 95%
1g
$ 631.00

American Custom Chemicals Corporation
2-PHENYL-CYCLOPROPANECARBOXALDEHYDE 95.00%
5MG
$ 501.24

Alichem
2-Phenylcyclopropanecarbaldehyde
1g
$ 560.32

Total 14 raw suppliers

Chemical Property of 2-Phenylcyclopropane-1-carbaldehyde

Chemical Property:

Boiling Point:240.6±29.0 °C(Predicted)
PSA：17.07000
Density:1.178±0.06 g/cm3(Predicted)
LogP:1.98900
Storage Temp.:2-8°C
XLogP3:1.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:146.073164938
Heavy Atom Count:11
Complexity:147

Purity/Quality:

98%,99%, ^*data from raw suppliers

2-PHENYLCYCLOPROPANECARBALDEHYDE Aldrich ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C(C1C2=CC=CC=C2)C=O

Technology Process of 2-Phenylcyclopropane-1-carbaldehyde

There total 54 articles about 2-Phenylcyclopropane-1-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: 95.0%