Anilinoacetic acid

• CAS: 103-01-5
• Catalog Number: ACM103015
• Category: Other Products
• Molecular Weight: 151.16
• Molecular Formula: C₈H₉NO₂
• Synonyms: AURORA KA-3653;ANILINOACETIC ACID;H-PHENYLGLY-OH;AKOS B003332;RARECHEM AL BO 1139;N-PHENYLGLYCIN;N-PHENYLGLYCINE;N-PHENYL-GLY-OH
• Melting Point: 121-123°C(lit.)
• Safety Description: 22-24/25

Custom Q&A

What is the molecular formula of Anilinoacetic acid?

The molecular formula of Anilinoacetic acid is C8H9NO2.

What is the molecular weight of Anilinoacetic acid?

The molecular weight of Anilinoacetic acid is 151.16 g/mol.

What is the IUPAC name of Anilinoacetic acid?

The IUPAC name of Anilinoacetic acid is 2-anilinoacetic acid.

What is the InChIKey of Anilinoacetic acid?

The InChIKey of Anilinoacetic acid is NPKSPKHJBVJUKB-UHFFFAOYSA-N.

What is the Canonical SMILES representation of Anilinoacetic acid?

The Canonical SMILES representation of Anilinoacetic acid is C1=CC=C(C=C1)NCC(=O)O.

What is the CAS number of Anilinoacetic acid?

The CAS number of Anilinoacetic acid is 103-01-5.

What is the XLogP3 value of Anilinoacetic acid?

The XLogP3 value of Anilinoacetic acid is 0.6.

How many hydrogen bond donor counts does Anilinoacetic acid have?

Anilinoacetic acid has 2 hydrogen bond donor counts.

What is the topological polar surface area of Anilinoacetic acid?

The topological polar surface area of Anilinoacetic acid is 49.3 Ų.

How many heavy atoms does Anilinoacetic acid contain?

Anilinoacetic acid contains 11 heavy atoms.

Synthetic Use

Upstream Synthesis Route 1

• 3009-97-0

• 103-01-5

Reference: [1]v.Miller; Ploechl; Hofer
[Chemische Berichte, 1892, vol. 25, p. 2028]
[2]Current Patent Assignee: Gold- u. Silber-Scheideanst. - DE169186, 1800, C
[3]Rayavarapu, Pratima; Shah, Shikha; Sunder, Avinash Vellore; Wangikar, Pramod P.
[Process Biochemistry, 2020, vol. 94, p. 289 - 296]

Downstream Synthesis Route 1

• 103-01-5

• 14328-51-9

Reference: [1] Patent: US5338726, 1994, A,

Downstream Synthesis Route 2

• 67-56-1
• 103-01-5

• 23284-84-6

Reference: [1]Current Patent Assignee: MERCK & CO INC - US2005/107355, 2005, A1
Location in patent: Page/Page column 29
[2]Nishimoto, Sei-ichi; Tada, Hiroaki; Kagiya, Tsutomu
[Journal of the Chemical Society. Perkin transactions II, 1983, p. 873 - 878]
[3]Fischer,E.; Gluud
[Justus Liebigs Annalen der Chemie, 1909, vol. 369, p. 250]

Downstream Synthesis Route 3

• 103-01-5
• 79-11-8

• 1137-73-1

Reference: [1]Hausdoerfer
[Chemische Berichte, 1889, vol. 22, p. 1799][Chemische Berichte, 1890, vol. 23, p. 1990]
[2]Bischoff; Hausdoerfer
[Chemische Berichte, 1890, vol. 23, p. 1998][Chemische Berichte, 1892, vol. 25, p. 2284,2287]
[3]Vorlaender; Mumme
[Chemische Berichte, 1901, vol. 34, p. 1647]
[4]Johnson; Bengis
[Journal of the American Chemical Society, 1911, vol. 33, p. 745]

* For details of the synthesis route, please refer to the original source to ensure accuracy.