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1,1'-Biphenyl-2-acetic acid

CAS 14676-52-9C14H12O2MW 212.24

1,1'-Biphenyl-2-acetic acid (CAS 14676-52-9) — formula C14H12O2, molecular weight 212.24; category organic chemicals.

Product Overview

CAS Number14676-52-9
Molecular FormulaC14H12O2
Molecular Weight212.24
LogP3.2
CategoryOrganic Chemicals

Technical Profile

What this product is

1,1'-Biphenyl-2-acetic acid is a carbon-based organic compound with CAS registry number 14676-52-9 and molecular formula C14H12O2 (molecular weight 212.24), belonging to the organic chemicals segment of chemical raw materials.

Identification

CAS number: 14676-52-9

Its molecular formula C14H12O2 comprises 14 C, 12 H, 2 O atoms.

Also known as: 1,1'-Biphenyl-2-acetic acid · 1,1'-联苯-2-乙酸

Category: organic chemicals

Frequently Asked Questions

What is the CAS number of 1,1'-Biphenyl-2-acetic acid?

The CAS registry number of 1,1'-Biphenyl-2-acetic acid is 14676-52-9.

What is the molecular formula and molecular weight of 1,1'-Biphenyl-2-acetic acid?

Molecular formula C14H12O2, molecular weight 212.24.

What other names is 1,1'-Biphenyl-2-acetic acid known by?

It is also registered under: 1,1'-Biphenyl-2-acetic acid, 1,1'-联苯-2-乙酸.

Which category does 1,1'-Biphenyl-2-acetic acid belong to?

Category: Organic Chemicals.

PubChem Public Data

Independent reference data for 1,1'-Biphenyl-2-acetic acid (CAS 14676-52-9), compiled from public chemistry databases.

Registry identifiers across databases

CAS Registry Number14676-52-9
PubChem CID263373
Molecular formulaC14H12O2
IUPAC name2-(2-phenylphenyl)acetic acid

Computed descriptors

Molecular Weight212.24
XLogP33.2
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count3
Exact Mass212.083729621
Monoisotopic Mass212.083729621
Topological Polar Surface Area37.3
Heavy Atom Count16

Documented uses on record

  • Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions. They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects.

Synonyms and trade names

Biphenylacetic acid; Biphenylylacetic acid; 51317-25-0; RefChem:85597; 14676-52-9; 2-([1,1'-Biphenyl]-2-yl)acetic acid; 2-Biphenylacetic acid; 2-(2-phenylphenyl)acetic acid; biphenyl-2-ylacetic acid; 1,1'-Biphenyl-2-acetic acid; MFCD06208460; [1,1'-Biphenyl]-2-acetic acid; biphenyl acetic acid; Fenbufen Impurity 15; 2-([1,1'-Biphenyl]-2-yl)aceticacid; (biphenyl-2-yl)acetic acid

What the public record says

1,1'-Biphenyl-2-acetic acid · CAS 14676-52-9 · C14H12O2.

Source: PubChem / Wikidata; the batch COA governs where values differ.

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Supplier: Jinan Shenghe Chemical Co., Ltd.

中文页面: 1,1'-联苯-2-乙酸

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