Bicyclo[1.1.1]pentane-1-carboxylic Acid

Base Information

Chemical Name:Bicyclo[1.1.1]pentane-1-carboxylic Acid
CAS No.:22287-28-1
Molecular Formula:C6H8O2
Molecular Weight:112.128
Hs Code.:2916200090
European Community (EC) Number:819-278-7
Nikkaji Number:J1.123.365A
Mol file:22287-28-1.mol

Synonyms:Bicyclo[1.1.1]pentane-1-carboxylic Acid;22287-28-1;MFCD19228106;SCHEMBL8717720;AMY32624;bicyclo(1,1,1)pentane-1-carboxylic;bicyclo[1.1.1]pentanecarboxylic acid;AKOS006378583;AKOS006387670;SB40657;SS-4732;Bicyclo[1.1.1]pentane-1-carboxylicAcid;SY042507;CS-0036907;bicyclo[1.1.1]?pentane-?1-?carboxylic acid;EN300-83811;P12599;EN300-7269000;A857893;Z1205493798

Suppliers and Price of Bicyclo[1.1.1]pentane-1-carboxylic Acid

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
Bicyclo[1.1.1]pentane-1-carboxylicacid
1mg
$ 65.00

SynQuest Laboratories
Bicyclo[1.1.1]pentane-1-carboxylic acid
250 mg
$ 720.00

SynQuest Laboratories
Bicyclo[1.1.1]pentane-1-carboxylic acid
100 mg
$ 448.00

Crysdot
Bicyclo[1.1.1]pentane-1-carboxylicacid 95+%
100mg
$ 365.00

Crysdot
Bicyclo[1.1.1]pentane-1-carboxylicacid 95+%
250mg
$ 550.00

Chemenu
bicyclo[1.1.1]pentane-1-carboxylicacid 95%+
1g
$ 929.00

Biosynth Carbosynth
Bicyclo[1,1,1]pentane-1-carboxylic acid
25 mg
$ 700.00

Biosynth Carbosynth
Bicyclo[1,1,1]pentane-1-carboxylic acid
10 mg
$ 500.00

Biosynth Carbosynth
Bicyclo[1,1,1]pentane-1-carboxylic acid
2 mg
$ 300.00

Biosynth Carbosynth
Bicyclo[1,1,1]pentane-1-carboxylic acid
1 mg
$ 200.00

Total 25 raw suppliers

Chemical Property of Bicyclo[1.1.1]pentane-1-carboxylic Acid

Chemical Property:

Melting Point:59 - 59.7 °C
Boiling Point:224.3±8.0 °C(Predicted)
PKA:4.99±0.20(Predicted)
PSA：37.30000
Density:1.461±0.06 g/cm3(Predicted)
LogP:0.87110
XLogP3:0.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:112.052429494
Heavy Atom Count:8
Complexity:134

Purity/Quality:

99%, ^*data from raw suppliers

Bicyclo[1.1.1]pentane-1-carboxylicacid ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1C2CC1(C2)C(=O)O

Technology Process of Bicyclo[1.1.1]pentane-1-carboxylic Acid

There total 3 articles about Bicyclo[1.1.1]pentane-1-carboxylic Acid 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:

: 124-38-9,18923-20-1
carbon dioxide

: 98585-81-0
Bicyclo<1.1.1>pent-1-ylphenylthioether

: 22287-28-1
bicyclo[1.1.1]pentane-1-carboxylic acid

: 65-85-0,8013-63-6
benzoic acid

Guidance literature:: With lithium 4,4′-di(tert-butyl)biphenyl; Yield given. Multistep reaction. Title compound not separated from byproducts; 1.) THF, -65 to -55 deg C, 45 min, 2.) -78 deg C;
DOI:10.1021/ja00162a022

Reference yield:

: 60-29-7,927820-24-4
diethyl ether

: 35634-10-7
[1.1.1]propellane

: 22287-28-1
bicyclo[1.1.1]pentane-1-carboxylic acid

: 137335-61-6
1-acetylbicyclo<1.1.1>pentane

: 137335-60-5
1-(1-acetoxyethyl)bicyclo<1.1.1>pentane

: 137335-08-1
<2>staffane-3-carboxylic acid

Guidance literature:: With ruthenium(IV) oxide; Perbenzoic acid; Multistep reaction. Further byproducts given. Yields of byproduct given; 1.) irrad., 8 h, 2.) CCl₄, Chlorox;
DOI:10.1021/ja00028a029

Reference yield:

: 164795-72-6
1-bromo-3-(4,4-dimethyl-2-oxazolinyl)bicyclo<1.1.1>pentane

: 22287-28-1
bicyclo[1.1.1]pentane-1-carboxylic acid

: 146038-53-1
3-fluorobicyclo<1.1.1>pentane-1-carboxylic acid

Guidance literature:: With hydrogenchloride; tert.-butyl lithium; 2-fluoro-3,3-dimethyl-2,3-dihydro-1,2-benzisothiazole-1,1-dioxide; Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts;