4-(Phenylmethyl)benzeneacetic acid

Base Information

Chemical Name:4-(Phenylmethyl)benzeneacetic acid
CAS No.:35889-03-3
Molecular Formula:C15H14O2
Molecular Weight:226.275
Hs Code.:
DSSTox Substance ID:DTXSID701296372

Synonyms:35889-03-3;4-(Phenylmethyl)benzeneacetic acid;SCHEMBL5696415;DTXSID701296372;AKOS002392927;FT-0756134

Suppliers and Price of 4-(Phenylmethyl)benzeneacetic acid

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 4-(Phenylmethyl)benzeneacetic acid

Chemical Property:

XLogP3:3.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:226.099379685
Heavy Atom Count:17
Complexity:235

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)CC2=CC=C(C=C2)CC(=O)O

Technology Process of 4-(Phenylmethyl)benzeneacetic acid

There total 6 articles about 4-(Phenylmethyl)benzeneacetic 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: 58.0%

: 26077-80-5
(4-benzoylphenyl)acetic acid

: 35889-03-3
2-(4-benzylphenyl)acetic acid

Guidance literature:: With hydrazine hydrate; potassium hydroxide; In ethylene glycol; at 110 - 180 ℃; for 22h;
DOI:10.1021/jm201327p

Reference yield:

: 101430-99-3
1-(4-benzyl-phenyl)-propan-2-ol

: 620-86-0
4-Benzylbenzoic acid

: 35889-03-3
2-(4-benzylphenyl)acetic acid

: 64-19-7,77671-22-8
acetic acid

Guidance literature:

Reference yield:

: 134-84-9
4-Methylbenzophenone

: 35889-03-3
2-(4-benzylphenyl)acetic acid

Guidance literature:: Multi-step reaction with 4 steps

1: N-Bromosuccinimide; dibenzoyl peroxide / tetrachloromethane / 4.17 h / 20 °C / Reflux

2: 1,4-dioxane; water / 2 h / Reflux

3: ethanol; sodium hydroxide / water / 2 h / Reflux

4: hydrazine hydrate; potassium hydroxide / ethylene glycol / 22 h / 110 - 180 °C

With N-Bromosuccinimide; ethanol; hydrazine hydrate; potassium hydroxide; sodium hydroxide; dibenzoyl peroxide; In 1,4-dioxane; tetrachloromethane; water; ethylene glycol;
DOI:10.1021/jm201327p