2-(3,3-dimethylbutan-2-ylcarbamoyl)benzoic Acid

Base Information

Chemical Name:2-(3,3-dimethylbutan-2-ylcarbamoyl)benzoic Acid
CAS No.:3907-04-8
Molecular Formula:C₁₄H₁₉NO₃
Molecular Weight:249.31
Hs Code.:2924299090
European Community (EC) Number:688-637-6
DSSTox Substance ID:DTXSID401346522
Mol file:3907-04-8.mol

Synonyms:3907-04-8;N-(1,2,2-TriMethyl-propyl)-phthalaMic acid;2-{[(1,2,2-trimethylpropyl)amino]carbonyl}benzoic acid;(+)-n-pinacolylphthalamic acid;2-(3,3-dimethylbutan-2-ylcarbamoyl)benzoic Acid;DTXSID401346522;2-(1,2,2-Trimethylpropylcarbamoyl)benzoic acid;2-[(3,3-Dimethyl-2-butanyl)carbamoyl]benzoic acid

Suppliers and Price of 2-(3,3-dimethylbutan-2-ylcarbamoyl)benzoic 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

Sigma-Aldrich
(+)-N-PINACOLYLPHTHALAMIC ACID AldrichCPR
250mg
$ 57.00

Sigma-Aldrich
(-)-N-PINACOLYLPHTHALAMIC ACID AldrichCPR
250mg
$ 55.10

American Custom Chemicals Corporation
(+)-N-PINACOLYLPHTHALAMIC ACID 95.00%
250MG
$ 150.00

Total 4 raw suppliers

Chemical Property of 2-(3,3-dimethylbutan-2-ylcarbamoyl)benzoic Acid

Chemical Property:

PSA：69.89000
LogP:3.12400
XLogP3:2.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:249.13649347
Heavy Atom Count:18
Complexity:320

Purity/Quality:

99% ^*data from raw suppliers

(+)-N-PINACOLYLPHTHALAMIC ACID AldrichCPR ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C(C)(C)C)NC(=O)C1=CC=CC=C1C(=O)O

Technology Process of 2-(3,3-dimethylbutan-2-ylcarbamoyl)benzoic Acid

There total 6 articles about 2-(3,3-dimethylbutan-2-ylcarbamoyl)benzoic 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:

: 141294-37-3
(R,R)-N-(1,2,2-trimethylpropyl)phenylethyl-1-amine α-methylbenzylamine

: 3907-04-8
Pinakolylamin-phthalsaeuremonoamid

Guidance literature:: Multi-step reaction with 2 steps

1: H₂ / Pd(OH)2-C / ethanol / 7500.6 Torr / Ambient temperature

2: Et₃N / acetone

With hydrogen; triethylamine; palladium hydroxide - carbon; In ethanol; acetone;

Reference yield:

: 75-97-8
3,3-dimethyl-butan-2-one

: 3907-04-8
Pinakolylamin-phthalsaeuremonoamid

Guidance literature:: Multi-step reaction with 3 steps

1: TsOH / benzene

2: H₂ / Pd(OH)2-C / ethanol / 7500.6 Torr / Ambient temperature

3: Et₃N / acetone

With hydrogen; toluene-4-sulfonic acid; triethylamine; palladium hydroxide - carbon; In ethanol; acetone; benzene;

Reference yield:

: 141393-92-2
(R)-α-methyl-N-(1,2,2-trimethylpropylidene)benzenemethanamine

: 3907-04-8
Pinakolylamin-phthalsaeuremonoamid

Guidance literature:: Multi-step reaction with 2 steps

1: H₂ / Pd(OH)2-C / ethanol / 7500.6 Torr / Ambient temperature

2: Et₃N / acetone

With hydrogen; triethylamine; palladium hydroxide - carbon; In ethanol; acetone;