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(1R,2S)-N-((2-Hydroxy-2-phenyl)-1-methyl-ethyl)-N-methylformamid is a complex organic compound with a molecular formula of C12H17NO2. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it is characterized by the presence of a hydroxyl group (-OH) and a phenyl ring (C6H5) attached to a 1-methyl-ethyl group. The compound also features a formamidine functional group, which consists of a nitrogen atom bonded to a formyl group (-CHO) and a methyl group (-CH3). This specific arrangement of atoms and functional groups gives the compound unique chemical properties and potential applications in various fields, such as pharmaceuticals or chemical research.

1630-35-9

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1630-35-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1630-35-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,3 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1630-35:
(6*1)+(5*6)+(4*3)+(3*0)+(2*3)+(1*5)=59
59 % 10 = 9
So 1630-35-9 is a valid CAS Registry Number.

1630-35-9Relevant academic research and scientific papers

A novel type of N-formylation and related reactions of amines via cyanides and esters as formylating agents

Bao, Kai,Zhang, Weige,Bu, Xiujuan,Song, Zhichun,Zhang, Liang,Cheng, Maosheng

body text, p. 5429 - 5431 (2009/03/11)

A novel N-formylation and related reactions proceed from cyanides promoted by esters. The Royal Society of Chemistry.

A PROCESS FOR THE PREPARATION OF R-(-)-N, α-DIMETHYLPHENETHYLAMINE (LEVMETAMFETAMINE) OR S-(+)-N, α-DIMETHYLPHENETHYLAMINE (METHAMPHETAMINE) FROM d-EPHEDRINE OR L-EPHEDRINE RESPECTIVELY

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Page/Page column 16, (2008/06/13)

A process for synthesis of R-(-)-N, α -Dimethylphenethylamine (Levmetamfetamine, formula I), or S-(+)-N, α - Dimethyl phenethylamine (Methamphetamine, formula II ), from d-ephedrine of formula III or l-ephedrine formula IV, the process comprising the steps of (a) acylating the d- or l-ephedrine base of formula III or formula IV with an acylating agent to make a reaction mixture containing a N- acylated ephedrines of formula V or formula VI ; (b) deoxygenation of N-acylated ephedrines to make the compound of the formula VII or Formula VIII by using Raney Nickel catalyst ; and (c) acid hydrolysis of the above deoxygenated products to get the levmetamfetamine or methamphetamine.

Reactions of (-)-Ephedrine, (+)-Norpseudoephedrine and Derivatives with N,N-Dimethylacetamid-dimethylacetal and N,N-Dimethylformamid-dimethylacetal

Koehl, M,Spreitzer, H.,Fleischhacker, W.

, p. 911 - 918 (2007/10/02)

The reactivity of (-)-ephedrine (2) and (+)-norpseudoephedrine (3) towards the amid-acetals 1 a/b has been studied.Both 2 and 3 were acetylated resp. formylated at first at the amino group.Nevertheless, derivatives of 2 and 3 possessing a trisubstituted amino group react with 1 a in a sigmatropic rearrangement to ortho substituted dimethylcarbamoylmethyl derivatives.By subsequent reduction with lithiumaluminiumhydride the aromatic compounds 8, 13, and 18 with two aminoethyl groups are easily available.In contrast to these results 1 b did not furnish any rearrangement products. Keywords. (-)-Ephedrine; (+)-Norpseudoephedrine; N,N-Dimethylacetamid-dimethylacetal; N,N-Dimethylformamid-dimethylacetal; Sympathomimetic effects; Sigmatropic rearrangements.

Rapid and Selective Formylation With Pentafluorophenyl Formate

Kisfaludy, Lajos,Oetvoes, Laszlo

, p. 510 (2007/10/02)

Pentafluorophenyl formate reacts smoothly with N-nucleophiles under mild conditions to give the N-formyl derivatives, whereas O- and S-nucleophiles remain unaffected even in the presence of a tertiary base.

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