32370-44-8

Basic information

• Product Name: Chromium, (aminophenylmethylene)pentacarbonyl-, (OC-6-21)-
• CAS NO: 32370-44-8
• Molecular Weight: 297.187
• Mol File: 32370-44-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Chromium, (aminophenylmethylene)pentacarbonyl-, (OC-6-21)-(CAS DataBase Reference)
• NIST Chemistry Reference: Chromium, (aminophenylmethylene)pentacarbonyl-, (OC-6-21)-(32370-44-8)
• EPA Substance Registry System: Chromium, (aminophenylmethylene)pentacarbonyl-, (OC-6-21)-(32370-44-8)

Safety Data

• Hazardous Substances Data: 32370-44-8(Hazardous Substances Data)

Upstream product

• 27436-93-7 pentacarbonyl(1-methoxybenzylidene)chromium⁽⁰⁾ 
• 121809-06-1 {(O-acetyl ethanimidato)phenylcarbene}pentacarbonylchromium⁽⁰⁾ 
• 124-41-4 sodium methylate 
• 15975-93-6 pentacarbonyl((methyl)((tetramethylammonio)oxy)carbene)chromium⁽⁰⁾ 
• 506-96-7 Acetyl bromide 
• 621-84-1 O-benzyl carbamate 

Downstream Products

• 31265-22-2 trans-(CO)5CrHNCHPh 
• 121809-06-1 {(O-acetyl ethanimidato)phenylcarbene}pentacarbonylchromium⁽⁰⁾ 
• 117497-96-8 (3-t-butyl-3-pivaloyl-1-phenyl-2-azaallenyl)pentacarbonylchromium 
• 19706-01-5 (benzonitrile)(pentacarbonyl)chromium 
• 117497-89-9 pentacarbonyl(1,3-diphenyl-2-azaallenyl)chromium 
• 117497-95-7 {(O-benzoyl benzimido)phenylmethylene}pentacarbonylchromium 
• 117497-90-2 pentacarbonyl{3-(4-methoxyphenyl)-1-phenyl-2-azaallenyl}chromium 
• 117497-92-4 pentacarbonyl(1-phenyl-3-trans-styryl-2-azaallenyl)chromium 
• 117497-95-7 {3-(benzoyloxy)-1,3-diphenyl-2-azaallenyl}pentacarbonylchromium 
• 19706-05-9 pentacarbonyl(cyclohexylisocyanide)chromium 
• 15227-70-0 cis(cyclic-C₆H₁₁NC)2Cr(CO)4 
• 83576-85-6 cis-(α-aminobenzylidene)tetracarbonyl(cyclohexylisocyano)chromium 
• 119209-09-5 tetracarbonyl{2-(cylohexylimino)-1-imino-1-phenylethane}chromium 
• 117497-93-5 pentacarbonyl{3-(4-formylphenyl)-1-phenyl-2-azaallenyl}chromium 

Relevant articles and documents

Photolytic reactions of chromium aminocarbene complexes. Conversion of amides to α-amino acids

A variety of tertiary amides was converted to chromium aminocarbene complexes by reaction with Na2Cr(CO)5 and trimethylsilyl chloride. Photolysis of these carbene complexes in methanol or tert-butyl alcohol solvent produced α-amino esters in good to excellent yield. Aminocarbene complexes containing chiral oxazolidine groups were synthesized and photolyzed in alcohol to produce chiral α-amino esters in 50-93% de. Pentacarbonyl[(dibenzylamino)(methyl)carbene]chromium(0) was prepared in high yield by the N-benzylation of the corresponding monobenzyl amino complex. Base-assisted alkylation of the methyl group with a variety of halides followed by photolysis in methanol produced the alkylated alanine methyl ester in excellent overall yield. Other aminocarbene complexes underwent similar reactions. With chiral, optically active aminocarbene complexes, the alkylated alanine derivative was produced with high diastereoselectivity.