N-(Allyloxycarbonyloxy)succinimide

• CAS: 135544-68-2
• Catalog Number: ACM135544682-1
• Category: Allyloxycarbonylation (Alloc) Reagents
• Molecular Weight: 199.16
• Molecular Formula: C8H9NO5
• Synonyms: Allyl N-succinimidyl carbonate
• Density: 1.287 g/mL at 25 °C
• Physical State: Liquid

Custom Q&A

What is the molecular formula of 2,6-Dichlorobenzonitrile?

The molecular formula of 2,6-Dichlorobenzonitrile is C7H3Cl2N.

How is 2,6-Dichlorobenzonitrile primarily used?

2,6-Dichlorobenzonitrile is used as a herbicide.

What is the molecular weight of 2,6-Dichlorobenzonitrile?

The molecular weight of 2,6-Dichlorobenzonitrile is 172.01 g/mol.

What are some synonyms for 2,6-Dichlorobenzonitrile?

Some synonyms for 2,6-Dichlorobenzonitrile include dichlobenil, Benzonitrile, 2,6-dichloro, and Dichlobanil.

What are the immediate steps that should be taken to limit the spread of 2,6-Dichlorobenzonitrile to the environment?

Immediate steps should be taken to limit the spread of 2,6-Dichlorobenzonitrile to the environment.

What is the primary hazard associated with 2,6-Dichlorobenzonitrile?

The primary hazard associated with 2,6-Dichlorobenzonitrile is the threat to the environment.

What is the InChIKey for 2,6-Dichlorobenzonitrile?

The InChIKey for 2,6-Dichlorobenzonitrile is YOYAIZYFCNQIRF-UHFFFAOYSA-N.

How is 2,6-Dichlorobenzonitrile described in the Toxin and Toxin Target Database (T3DB)?

2,6-Dichlorobenzonitrile is described as a chemical compound of cyanide and a herbicide in the Toxin and Toxin Target Database.

What is the IUPAC Name of 2,6-Dichlorobenzonitrile?

The IUPAC Name of 2,6-Dichlorobenzonitrile is 2,6-dichlorobenzonitrile.

What is the role of 2,6-Dichlorobenzonitrile according to CAMEO Chemicals?

2,6-Dichlorobenzonitrile is a cellulose synthesis inhibitor used as a pre-emergent and early post-emergent herbicide according to CAMEO Chemicals.

Synthetic Use

Upstream Synthesis Route 1

• 74124-79-1
• 107-18-6

• 135544-68-2

Reference: [1] Chemistry - A European Journal, 2014, vol. 20, # 50, p. 16502 - 16508

Upstream Synthesis Route 2

• 6066-82-6
• 2937-50-0

• 135544-68-2

Reference: [1] Organic letters, 2003, vol. 5, # 3, p. 247 - 250

Downstream Synthesis Route 1

• 135544-68-2
• 60-23-1

• 135920-21-7

Reference: [1]Tetrahedron Letters,1981,vol. 22,p. 3489 - 3492

Downstream Synthesis Route 2

• 135544-68-2
• 4761-34-6

• 162893-14-3

Reference: [1]Recueil des Travaux Chimiques des Pays-Bas,1995,vol. 114,p. 27 - 34

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