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N,1-dimethylpropylamine, also known as 2-methyl-2-butanamine, is a secondary aliphatic amine that is sec-butylamine substituted by a methyl group at the N atom. It is a metabolite observed in cancer metabolism.

7713-69-1

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7713-69-1 Usage

Uses

Used in Pharmaceutical Industry:
N,1-dimethylpropylamine is used as a pharmaceutical intermediate for the synthesis of various drugs and medications. Its unique chemical structure allows it to be a versatile building block in the development of new therapeutic agents.
Used in Chemical Industry:
N,1-dimethylpropylamine is used as a chemical intermediate in the production of various chemicals, including agrochemicals, surfactants, and other specialty chemicals. Its reactivity and functional groups make it a valuable component in the synthesis of a wide range of compounds.
Used in Research:
N,1-dimethylpropylamine is used as a research tool in the study of cancer metabolism and the development of new cancer therapies. Its presence in cancer metabolism makes it a potential target for the discovery of novel anticancer agents and the understanding of the underlying metabolic pathways in cancer cells.

Check Digit Verification of cas no

The CAS Registry Mumber 7713-69-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,1 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7713-69:
(6*7)+(5*7)+(4*1)+(3*3)+(2*6)+(1*9)=111
111 % 10 = 1
So 7713-69-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H13N/c1-4-5(2)6-3/h5-6H,4H2,1-3H3

7713-69-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methylbutan-2-amine

1.2 Other means of identification

Product number -
Other names 2-Butanamine, N-methyl-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7713-69-1 SDS

7713-69-1Relevant academic research and scientific papers

Photometric Characterization of the Reductive Amination Scope of the Imine Reductases from Streptomyces tsukubaensis and Streptomyces ipomoeae

Matzel, Philipp,Krautschick, Lukas,H?hne, Matthias

, p. 2022 - 2027 (2017/10/07)

Imine reductases (IREDs) have emerged as promising enzymes for the asymmetric synthesis of secondary and tertiary amines starting from carbonyl substrates. Screening the substrate specificity of the reductive amination reaction is usually performed by time-consuming GC analytics. We found two highly active IREDs in our enzyme collection, IR-20 from Streptomyces tsukubaensis and IR-Sip from Streptomyces ipomoeae, that allowed a comprehensive substrate screening with a photometric NADPH assay. We screened 39 carbonyl substrates combined with 17 amines as nucleophiles. Activity data from 663 combinations provided a clear picture about substrate specificity and capabilities in the reductive amination of these enzymes. Besides aliphatic aldehydes, the IREDs accepted various cyclic (C4–C8) and acyclic ketones, preferentially with methylamine. IR-Sip also accepted a range of primary and secondary amines as nucleophiles. In biocatalytic reactions, IR-Sip converted (R)-3-methylcyclohexanone with dimethylamine or pyrrolidine with high diastereoselectivity (>94–96 % de). The nucleophile acceptor spectrum depended on the carbonyl substrate employed. The conversion of well-accepted substrates could also be detected if crude lysates were employed as the enzyme source.

Synthesis of N-methyl-N-(1-methylpropyl)-1-(2-chlorophenyl)-isoquinoline-3-[11C]ca rboxamide ([11C-carbonyl]PK11195) and some analogues using [11C]carbon monoxide and 1-(2-chlorophenyl)isoquinolin-3-yl triflate

Rahman, Obaidur,Kihlberg, Tor,Langstroem, Bengt

, p. 2699 - 2703 (2007/10/03)

The benzodiazepine receptor ligand, N-methyl-N-(1-methylpropyl)-1-(2-chlorophenyl)isoquinoline-3-carboxamide (PK11195), and five structurally related analogues were 11C-labelled via a palladium-mediated carbonylation using [11C]carbon monoxide, 1-(2-chlorophenyl)isoquinolin-3-yl trifluoromethanesulfonate and various amines. The 11C-labelled products were obtained with decay-corrected radiochemical yields in the range of 10-55% and with high specific radioactivity (e.g. 200-900 GBq μmol-1). The radiochemical purity of the final products exceeded 98%. In a typical experiment starting with 3.75 GBq [11C]carbon monoxide, 0.57 GBq of LC-purified products were obtained within 35 min of the start of the carbonylation reaction. For confirmation of the labelling position, N-(1-methylethyl)-1-(2-chlorophenyl)-isoquinoline-3-(13C)carboxamide was prepared and analysed by NMR. The precursor 1-(2-chlorophenyl)isoquinolin-3-yl trifluoromethanesulfonate was synthesised in five steps starting from 2-chlorobenzophenone. The precursor N-methyl-sec-butylamine was prepared from sec-butylamine by the reaction with ethyl chloroformate followed by reduction with LiAlH4. The non-radioactive reference compounds for the analogues were synthesised from 1-(2-chlorophenyl)isoquinoline-3-carboxylic acid and the appropriate amines.

ELECTROCHEMICAL REDUCTIVE AMINATION. I. AMINATION OF ALIPHATIC KETONES BY PRIMARY AMINES

Smirnov, Yu. D.,Tomilov, A. P.

, p. 42 - 48 (2007/10/02)

The reductive amination of aliphatic ketones in aqueous solutions of primary amines was realized by an electrochemical method.The best yields of the secondary amines were obtained at lead and cadmium cathodes in an aqueous electrolytic solution at pH 11-12.Elongation and branching in the carbon chain of the radicals both of the ketone and of the primary amine lead to a reduction in the yield of the secondary amine.The yield of the secondary amine is mainly determined by the rate of the chemical reaction leading to the formation of the azomethine compound, preceding the electrochemical reduction stage.

Ion-Dipole Complexes in the Unimolecular Reactions of Isolated Organic Ions. Effect of N-Methylation on Olefin and Amine Loss from Protonated Aliphatic Amines

Bowen, Richard D.,Harrison, Alex G.,Reiner, Eric J.

, p. 1009 - 1014 (2007/10/02)

The slow unimolecular fragmentation reactions os 18 gaseous protonated aliphatic amines of general formula R1NH(1+)R2R3 (R1=Prn, Pri, Bun, Bui, Bus, or But; R2,R3=H,CH3) are reported and discussed.Two decomposition routes are observed for a metastable ions R1NH(1+)R2R3.The first involves elimination of a neutral amine, R2R3NH, and formation of a carbocation, R1(1+), via a mechanism involving an incipient cation bound to the developing amine by an ion-dipole attraction.Rearrangement of the cation, to give thermodynamically more stable isomers, is feasible in these ion-dipole complexes.Further reorganization of the complexes leads to a species in which an incipient olefin 1-H> and an amine 2R3NH> are co-ordinated to a common proton.Dissociation of these proton-bound complexes, with retention of the proton by the developing amine, results in olefin loss, which is the secondreaction undergone by metastable ions R1NH(1+)R2R3.The relative abundance of amine expulsion is greater for protonated amines containing a primary alkyl group, R1, than is the case for isomeric ions containing secondary or tertiary alkyl groups.Progressive methylation of the nitrogen atom decreases the relative abundance of amine loss from R1NH(1+)R2R3, regardless of the nature of the principal alkyl group.These two trends are explained in terms of the energetics of the intermediates and products involved in the decomposition of the protonated amines.

THE ELECTROPHILIC AMINATION OF ORGANOLITHIUMS WITH METHYLLITHIUM COMPLEXES OF N-SUBSTITUTED METHOXYAMINES

Kokko, Bruce J.,Beak, Peter

, p. 561 - 564 (2007/10/02)

Three N-alkyl methoxyamine derivatives are shown to be effective as electrophilic reagents for the conversion of organolithiums to secondary amines.

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