69323-00-8

Basic information

• Product Name: 2-Propanol, 1-chloro-3-(methylphenylamino)-
• CAS NO: 69323-00-8
• Molecular Formula: C10H14ClNO
• Molecular Weight: 199.68
• Mol File: 69323-00-8.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: 2-Propanol, 1-chloro-3-(methylphenylamino)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propanol, 1-chloro-3-(methylphenylamino)-(69323-00-8)
• EPA Substance Registry System: 2-Propanol, 1-chloro-3-(methylphenylamino)-(69323-00-8)

Safety Data

• Hazardous Substances Data: 69323-00-8(Hazardous Substances Data)

Upstream product

• 100-61-8 N-methylaniline 
• 106-89-8 epichlorohydrin 

Downstream Products

• 1310582-00-3 3-(N-methyl-N-phenylamino)-1-(adenine-9-yl)propane-2-ol 
• 1310581-98-6 3-(N-methyl-N-phenylamino)-1-(uracil-1-yl)propane-2-ol 
• 1310581-96-4 3-(N-methyl-N-phenylamino)-1-(thymine-1-yl)propane-2-ol 
• 1021995-28-7 3-(N-methyl-N-phenylamino)-1-(morpholinopropan)-2-ol 
• 1310581-94-2 3-(N-methyl-N-phenylamino)-1-(pyrrolidin-1-yl)propan-2-ol 
• 1310581-93-1 3-(N-methyl-N-phenylamino)-1-(piperidin-1-yl)propan-2-ol 
• 1309922-47-1 1-(N-methyl-N-phenylamino)-3-thiocyanatopropan-2-yl acetate 
• 1260086-14-3 1-chloro-3-[methyl(phenyl)amino]propan-2-one 
• 14236-04-5 N-methyl-N-(oxiran-2-ylmethyl)aniline 
• 74229-88-2 1-chloro-3-[N-methyl-4-(4-nitro-phenylazo)-anilino]-propan-2-ol 

Relevant articles and documents

Phenalenyl in a different role: Catalytic activation through the nonbonding molecular orbital

We have demonstrated that the nonbonding molecular orbital (NBMO) of the phenalenyl (PLY) cation can be used as a Lewis acid catalyst for different organic transformations. Detailed computational and spectroscopic studies for the aminolysis reaction of ep

Fe(III) substituted Wells-Dawson type polyoxometalate: An efficient catalyst for ring opening of epoxides with aromatic amines

Various β-aminoalcohols were prepared by the ring opening reaction of epoxides with aromatic amines in the presence of Fe(III) substituted Wells-Dawson type polyoxometalate, α2-[(n-C4H 9)4N]7P2/

Simple synthesis of β-acetoxy thiocyanates from oxiranes

A convenient and simple method for the preparation of previously unknown β-acetoxy thiocyanates by regioselective ring opening of the corresponding oxiranes with thiocyanate anion followed by acetylation is described. The shorter reaction times, better yields of the products, and easy workup are the advantages of this methodology.