35256-85-0

Basic information

• Product Name: TEBUTAM
• Synonyms: n-benzyl-n-isopropylpivalamide;n-benzyl-n-isopropyltrimethylacetamide;s-15544;N-benzyl-N-isopropyl-2,2-dimethylpropionamide;2,6-DICHLOROBENZAMIDE PESTANAL;2,2-Dimethyl-N-isopropyl-N-(phenylmethyl)propanamide;2,2-Dimethyl-N-(1-methylethyl)-N-(phenylmethyl)propanamide (9ci);Brn 2838127
• CAS NO: 35256-85-0
• Molecular Formula: C₁₅H₂₃NO
• Molecular Weight: 233.35
• EINECS: 252-470-3
• Mol File: 35256-85-0.mol
• Article Data: 3

Chemical Properties

• Melting Point: <25℃
• Boiling Point: 340.4°Cat760mmHg
• Flash Point: 80 °C
• Appearance: /
• Density: 0.961g/cm³
• Vapor Pressure: 8.61E-05mmHg at 25°C
• Refractive Index: 1.504
• Storage Temp.: Refrigerator
• Solubility: Chloroform, Methanol
• PKA: -0.50±0.70(Predicted)
• BRN: 2838127
• CAS DataBase Reference: TEBUTAM(CAS DataBase Reference)
• NIST Chemistry Reference: TEBUTAM(35256-85-0)
• EPA Substance Registry System: TEBUTAM(35256-85-0)

Safety Data

• RIDADR: NA 1993 / PGIII
• WGK Germany: 2
• RTECS: UE3152000
• Hazardous Substances Data: 35256-85-0(Hazardous Substances Data)

Usage

Uses

Tebutam is used as herbicide and pesticide.

Definition

ChEBI: A monocarboxylic acid amide that is propanamide substituted by a benzyl and an isopropyl group at the nitrogen atom and two methyl groups at position 2. It is an agrochemical used as a herbicide.

InChI:InChI=1/C15H23NO/c1-12(2)16(14(17)15(3,4)5)11-13-9-7-6-8-10-13/h6-10,12H,11H2,1-5H3

Upstream product

• 110079-24-8 N-benzyl-N-chloropropan-2-amine 
• 630-19-3 pivalaldehyde 
• 102-97-6 Benzyl-isopropyl-amin 
• 3282-30-2 pivaloyl chloride 

Relevant articles and documents

One-pot synthesis of amides from aldehydes and amines via C-H bond activation

A one-pot synthesis of amides from aldheydes with N-chloroamines, prepared in situ from amines, has been developed. Both aliphatic and aromatic aldehydes and many types of mono- and disubstituted amines are tolerant in this transformation. This cross-coupling reaction appears simple and convenient, has a wide substrate scope and makes use of cheap, abundant, and easily available reagents.

Pre-emergent chemical method of combating unwanted vegetation

Undesired vegetation such as crabgrass, downey brome, giant foxtail, yellow foxtail, barnyard grass, flax and wild oats are combated by pre-emergent application of at least one compound belonging to a class of substituted N-benzyl amides of alkanoic and benzoic acids, particularly in the presence of seeds of such crops as cotton and soybeans. Illustrative of compounds which are very effective against several species of grasses as well as some broadleaf weeds in the presence of soybeans and cotton are two with the following structural formulas: EQU1 and EQU2