34021-55-1

Basic information

• Product Name: Benzamide, N-(1,1,3,3-tetramethylbutyl)-
• CAS NO: 34021-55-1
• Molecular Formula: C15H23NO
• Molecular Weight: 233.354
• Mol File: 34021-55-1.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzamide, N-(1,1,3,3-tetramethylbutyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, N-(1,1,3,3-tetramethylbutyl)-(34021-55-1)
• EPA Substance Registry System: Benzamide, N-(1,1,3,3-tetramethylbutyl)-(34021-55-1)

Safety Data

• Hazardous Substances Data: 34021-55-1(Hazardous Substances Data)

Upstream product

• 107-40-4 2,4,4-trimethylpent-2-ene 
• 100-47-0 benzonitrile 
• 107-45-9 tert-Octylamine 
• 65-85-0 benzoic acid 
• 591-50-4 iodobenzene 
• 14542-93-9 1,1,3,3-tetramethylbutane isonitrile 
• 108-86-1 bromobenzene 
• 582-25-2 Potassium benzoate 
• 100-52-7 benzaldehyde 
• 49707-52-0 1-phenyl-N-(2,4,4-trimethylpentan-2-yl)methanimine 
• 98-88-4 benzoyl chloride 

Downstream Products

• 34021-65-3 N-(4-Hydroxy-1,1,3,3-tetramethylbutyl)benzamid 

Relevant articles and documents

AMINE-BORANES AS BIFUNCTIONAL REAGENTS FOR DIRECT AMIDATION OF CARBOXYLIC ACIDS

The present invention generally relates to a process for selective and direct activation and subsequent amidation of aliphatic and aromatic carboxylic acids to afford an amide R3CONR1R2. That the process is capable of delivering gaseous or low-boiling point amines provides a major advantage over existing methodologies, which involves an intermediate of triacyloxyborane-amine complex [(R3CO2)3—B—NHR1R2]. This procedure readily produces primary, secondary, and tertiary amides, and is compatible with the chirality of the acid and amine involved. The preparation of known pharmaceutical molecules and intermediates has also been demonstrated.

A case study of Pd?Pd intramolecular interaction in a benzothiazole based palladacycle; catalytic activity toward amide synthesisviaan isocyanide insertion pathway

An acetate bridge benzothiazolepalladacycle containing a rare metallophilic intramolecular Pd?Pd interaction was synthesized and thoroughly characterized. The synthesized benzothiazolepalladacycle directly anchored on SBA-15 to form an efficient heterogen

Development of a process for triazine-promoted amidation of carboxylic acids

A process has been developed for the triazine-promoted amidation of carboxylic acids. We have identified 2,4,6-trichloro-1,3,5-triazine (cyanuric chloride) as a cost-effective reagent for this transformation. The procedure is a suitable alternative to traditional amidation processes when an acid chloride cannot be prepared from the corresponding carboxylic acid due to safety, stability, or handling concerns.