6200-21-1

Basic information

• Product Name: Benzenemethanol, 4-chloro-a-(1,1-dimethylethyl)-
• CAS NO: 6200-21-1
• Molecular Formula: C11H15ClO
• Molecular Weight: 198.692
• Mol File: 6200-21-1.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Benzenemethanol, 4-chloro-a-(1,1-dimethylethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, 4-chloro-a-(1,1-dimethylethyl)-(6200-21-1)
• EPA Substance Registry System: Benzenemethanol, 4-chloro-a-(1,1-dimethylethyl)-(6200-21-1)

Safety Data

• Hazardous Substances Data: 6200-21-1(Hazardous Substances Data)

Upstream product

• 123-62-6 propionic acid anhydride 
• 106-39-8 bromochlorobenzene 
• 26110-93-0 1-Chlor-4-(2,2-dimethylpropyl)benzol 
• 122-01-0 4-chloro-benzoyl chloride 
• 630-19-3 pivalaldehyde 
• 873-77-8 (4-chlorphenyl)magnesium bromide 
• 3282-30-2 pivaloyl chloride 
• 106-46-7 para-dichlorobenzene 
• 30314-42-2 1-(4-chlorophenyl)-2,2-dimethylpropan-1-one 
• 677-22-5 tert-butylmagnesium chloride 
• 104-88-1 4-chlorobenzaldehyde 

Downstream Products

• 109837-19-6 C₁₁H₁₅ClO 
• 6200-21-1 1-(4-Chlor-phenyl)-2,2-dimethyl-propan-1-ol 
• 1337920-82-7 C₁₄H₁₉ClO₂ 
• 872180-92-2 2-[1-(4-chlorophenyl)-2,2-dimethylpropoxy]-6-fluorobenzonitrile 
• 54953-06-9 4-Chlorpivalophenonazin 
• 26110-93-0 1-Chlor-4-(2,2-dimethylpropyl)benzol 
• 343844-08-6 meso-3,4-Bis(4-chlorphenyl)-2,2,5,5-tetramethylhexan 
• 68525-41-7 DL-3,4-Bis(4-chlorphenyl)-2,2,5,5-tetramethylhexan 
• 856780-72-8 1-chloro-4-(1-chloro-2,2-dimethyl-propyl)-benzene 
• 30314-42-2 1-(4-chlorophenyl)-2,2-dimethylpropan-1-one 
• 31006-91-4 β-tert.Butyl-p-chlor-zimtsaeure 
• 31006-79-8 β-p-chlorphenyl-β-tert-butyl-hydracrylsaeure-aethylester 
• 31006-80-1 β-p-chlorphenyl-β-tert-butyl-hydracrylsaeure 
• 120136-06-3 Toluene-4-sulfonic acid 1-(4-chloro-phenyl)-2,2-dimethyl-propyl ester 

Relevant articles and documents

Bi-aryl rotation in phenyl-dihydroimidazoquinoline catalysts for kinetic resolution of arylalkyl carbinols

Chiral nucleophilic catalysts, 6-aryl-phenyl-dihydroimidazoquinolines (PIQs), were designed, synthesised and applied to the kinetic resolution of arylalkyl carbinols with very high selectivity (S) factors (up to 530). Density functional theory calculations indicate that multiple noncovalent interactions play a key role in chiral recognition between 6-aryl-PIQ catalysts and chiral secondary alcohol substrates. The Royal Society of Chemistry 2014.

Enantioselective hydrogenation and transfer hydrogenation of bulky ketones catalysed by a ruthenium complex of a chiral tridentate ligand

A study on the enantioselective hydrogenation of tertiary alkyl ketones catalysed by a novel class of tridentate-Ru complex is reported. In contrast to the extensively studied [RuCl2(diphos)(di-primary amine)] complexes, this new class of hydro

2,4-DIAMINOQUINAZOLINES FOR SPINAL MUSCULAR ATROPHY

2,4-Diaminoquinazolines of formulae I-IV and VI (I, II, III, IV and VI) are useful for treating spinal muscular atrophy (SMA).