1-(tert-Butoxycarbonyl)imidazole

• CAS: 49761-82-2
• Catalog Number: ACM49761822-1
• Category: tert-Butoxycarbonylation (Boc) Reagents
• Molecular Weight: 168.19
• Molecular Formula: C8H12N2O2
• Boiling Point: 147-150 °C (lit.)
• Melting Point: 45-47 °C (lit.)
• Physical State: Solid

Custom Q&A

What is the molecular formula of 1-Methyl-3-nitro-1-nitrosoguanidine?

The molecular formula of 1-Methyl-3-nitro-1-nitrosoguanidine is C2H5N5O3.

What is the molecular weight of 1-Methyl-3-nitro-1-nitrosoguanidine?

The molecular weight of 1-Methyl-3-nitro-1-nitrosoguanidine is 147.09 g/mol.

How is 1-Methyl-3-nitro-1-nitrosoguanidine stored?

1-Methyl-3-nitro-1-nitrosoguanidine is usually stored frozen (below 32 °F) in polyethylene bottles that are tightly closed and contained in a metal can.

What are some synonyms for 1-Methyl-3-nitro-1-nitrosoguanidine?

Some synonyms for 1-Methyl-3-nitro-1-nitrosoguanidine are MNNG and Methylnitronitrosoguanidine.

What is the role of 1-Methyl-3-nitro-1-nitrosoguanidine?

1-Methyl-3-nitro-1-nitrosoguanidine has a role as an alkylating agent.

What safety precautions should be taken when handling 1-Methyl-3-nitro-1-nitrosoguanidine?

It is important to avoid skin contact and inhalation of vapors when handling 1-Methyl-3-nitro-1-nitrosoguanidine.

What is the InChIKey of 1-Methyl-3-nitro-1-nitrosoguanidine?

The InChIKey of 1-Methyl-3-nitro-1-nitrosoguanidine is VZUNGTLZRAYYDE-UHFFFAOYSA-N.

What is the melting point of 1-Methyl-3-nitro-1-nitrosoguanidine?

The melting point of 1-Methyl-3-nitro-1-nitrosoguanidine is 244 °F.

What are some other identifiers for 1-Methyl-3-nitro-1-nitrosoguanidine?

Some other identifiers for 1-Methyl-3-nitro-1-nitrosoguanidine include CAS number 70-25-7 and UNII number 12H3O2UGSF.

What are some of the computed properties of 1-Methyl-3-nitro-1-nitrosoguanidine?

Some computed properties of 1-Methyl-3-nitro-1-nitrosoguanidine include XLogP3-AA, hydrogen bond donor count, hydrogen bond acceptor count, rotatable bond count, exact mass, monoisotopic mass, and topological polar surface area.

Synthetic Use

Upstream Synthesis Route 1

• 288-32-4
• 24424-99-5

• 49761-82-2

Reference: [1] Tetrahedron Letters, 2008, vol. 49, # 16, p. 2527 - 2532

Upstream Synthesis Route 2

• 530-62-1
• 75-65-0

• 49761-82-2

Reference: [1] Tetrahedron Asymmetry, 2005, vol. 16, # 2, p. 297 - 301

Upstream Synthesis Route 3

• 288-32-4
• 98015-52-2

• 49761-82-2

Reference: [1] Synthesis, 1986, # 8, p. 627 - 632
[2] Journal of Organic Chemistry, 1985, vol. 50, # 20, p. 3951 - 3953
[3] Patent: US4725680, 1988, A,

Upstream Synthesis Route 4

• 288-32-4
• 98015-51-1

• 49761-82-2

Reference: [1]Synthesis,1986,p. 627 - 632

Upstream Synthesis Route 5

• 288-32-4
• 98015-52-2

• 49761-82-2

Reference: [1]Synthesis,1986,p. 627 - 632
[2]Journal of Organic Chemistry,1985,vol. 50,p. 3951 - 3953
[3]Patent: US4725680,1988,A

Downstream Synthesis Route 1

• 64-17-5
• 49761-82-2

• 27945-07-9

Reference: [1]Chemische Berichte,1962,vol. 95,p. 1284 - 1297

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