2-Methylbenzoxazole

• CAS: 95-21-6
• Catalog Number: ACM95216
• Category: Other Products
• Molecular Weight: 133.15
• Molecular Formula: C8H7NO
• Melting Point: 41861°C
• Flash Point: 75°C
• Density: 1.121
• Appearance: Yellow clear liquid
• Assay: 0.9999
• Packaging: 1 kg
• Refractive Index: 1.548
• Stability: Stable under normal temperatures and pressures. Light sensitive.
• Storage Conditions: Refrigerator

Custom Q&A

What is the molecular formula of 2-Methylbenzoxazole?

The molecular formula of 2-Methylbenzoxazole is C8H7NO.

What is the molecular weight of 2-Methylbenzoxazole?

The molecular weight of 2-Methylbenzoxazole is 133.15 g/mol.

What is the IUPAC name of 2-Methylbenzoxazole?

The IUPAC name of 2-Methylbenzoxazole is 2-methyl-1,3-benzoxazole.

What is the InChI of 2-Methylbenzoxazole?

The InChI of 2-Methylbenzoxazole is InChI=1S/C8H7NO/c1-6-9-7-4-2-3-5-8(7)10-6/h2-5H,1H3.

What is the InChIKey of 2-Methylbenzoxazole?

The InChIKey of 2-Methylbenzoxazole is DQSHFKPKFISSNM-UHFFFAOYSA-N.

What is the canonical SMILES of 2-Methylbenzoxazole?

The canonical SMILES of 2-Methylbenzoxazole is CC1=NC2=CC=CC=C2O1.

What is the CAS number of 2-Methylbenzoxazole?

The CAS number of 2-Methylbenzoxazole is 95-21-6.

What is the EC number of 2-Methylbenzoxazole?

The EC number of 2-Methylbenzoxazole is 202-399-9.

What is the FEMA number of 2-Methylbenzoxazole?

The FEMA number of 2-Methylbenzoxazole is 4398.

Synthetic Use

Downstream Synthesis Route 1

• 95-21-6

• 5676-56-2

Reference: [1] Pharmaceutical Chemistry Journal, 1976, vol. 10, # 12, p. 1631 - 1634[2] Khimiko-Farmatsevticheskii Zhurnal, 1976, vol. 10, # 12, p. 53 - 56

Downstream Synthesis Route 2

• 95-21-6

• 5676-60-8

Reference: [1] Journal of the Chemical Society, 1928, p. 121

Downstream Synthesis Route 3

• 95-21-6

• 5683-43-2
• 32046-51-8

Reference: [1] Tetrahedron Letters, 2007, vol. 48, # 49, p. 8659 - 8664

Downstream Synthesis Route 4

• 98-01-1
• 95-21-6

• 144154-59-6

Reference: [1]Angewandte Chemie - International Edition,2019,vol. 58,p. 10723 - 10726
Angew. Chem.,2019,vol. 134,p. 10833 - 10836,4
[2]Russian Journal of Organic Chemistry,2015,vol. 51,p. 1111 - 1113
Zhurnal Organicheskoi Khimii,2015,vol. 51,p. 1111 - 1113,3
[3]Justus Liebigs Annalen der Chemie,1956,vol. 600,p. 47,58
[4]PLoS ONE,2018,vol. 13

Downstream Synthesis Route 5

• 95-21-6
• 13673-62-6
• 80-40-0

• 15185-40-7

Reference: [1]Patent: US2310640,1934,

Downstream Synthesis Route 6

• 95-21-6
• 100-10-7

• 24675-13-6

Reference: [1]Chemical Communications,2014,vol. 50,p. 10284 - 10286
[2]Dyes and Pigments,2015,vol. 112,p. 255 - 261
[3]Journal of the Chemical Society,1948,p. 2147,2153
[4]Synthesis,1994,p. 973 - 978

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