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127729-35-5

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127729-35-5 Usage

Description

3-Aminopropyl(methyl)phosphinic acid HCl is an organic compound with the chemical formula C4H12ClNO2P. It is a derivative of aminopropylphosphinic acid, featuring a methyl group and a hydrochloride ion. 3-AMINOPROPYL(METHYL)PHOSPHINIC ACID HCL has potential applications in various fields due to its unique chemical structure and properties.

Uses

Used in Pharmaceutical Industry:
3-Aminopropyl(methyl)phosphinic acid HCl is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its ability to form stable complexes with metal ions makes it a promising candidate for the development of new drugs targeting metalloenzymes and metal-based diseases.
Used in Chemical Research:
In the field of chemical research, 3-Aminopropyl(methyl)phosphinic acid HCl is used as a reagent for the preparation of various organophosphorus compounds. Its unique structure allows for the development of new materials with potential applications in catalysis, materials science, and environmental chemistry.
Used in Neuropharmacology:
3-Aminopropyl(methyl)phosphinic acid HCl acts as a highly potent agonist of GABAB receptors. It has been shown to display sedative effects in mammals and may be used in the treatment of various addictions due to neurochemical imbalances. Its interaction with GABAB receptors can help modulate neuronal activity, providing a potential therapeutic approach for addiction treatment and other neurological disorders.
Used in Drug Delivery Systems:
Similar to gallotannin, 3-Aminopropyl(methyl)phosphinic acid HCl can be employed in the development of novel drug delivery systems. Its ability to form complexes with metal ions and its compatibility with various organic and inorganic materials make it a suitable candidate for improving the delivery, bioavailability, and therapeutic outcomes of various drugs.

Biological Activity

A very potent GABA B agonist, at least ten times more active than baclofen ((RS)-4-Amino-3-(4-chlorophenyl)butanoic acid ). Also GABA C antagonist.

Check Digit Verification of cas no

The CAS Registry Mumber 127729-35-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,7,2 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 127729-35:
(8*1)+(7*2)+(6*7)+(5*7)+(4*2)+(3*9)+(2*3)+(1*5)=145
145 % 10 = 5
So 127729-35-5 is a valid CAS Registry Number.
InChI:InChI=1/C4H12NO2P/c1-8(6,7)4-2-3-5/h2-5H2,1H3,(H,6,7)/p+1

127729-35-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name P-(3-aminopropyl)-P-methyl-phosphinic acid

1.2 Other means of identification

Product number -
Other names -

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:127729-35-5 SDS

127729-35-5Synthetic route

4-(n-nonyl)benzaldehyde
70972-98-4

4-(n-nonyl)benzaldehyde

3-aminopropyl(methyl)phosphinic acid
127729-35-5

3-aminopropyl(methyl)phosphinic acid

methyl-[3-(4-nonyl-benzylamino)-propyl]-phosphinic acid

methyl-[3-(4-nonyl-benzylamino)-propyl]-phosphinic acid

Conditions
ConditionsYield
With tetra(n-butyl)ammonium hydroxide; sodium cyanoborohydride In methanol at 50℃;
(1R)-1-[((3S,4S)-2,5-Dioxo-3,4-dibenzoyloxypyrrolidinyl)-oxycarbonyloxy]-2-methylpropyl 2-methylpropanoate
847353-26-8

(1R)-1-[((3S,4S)-2,5-Dioxo-3,4-dibenzoyloxypyrrolidinyl)-oxycarbonyloxy]-2-methylpropyl 2-methylpropanoate

3-aminopropyl(methyl)phosphinic acid
127729-35-5

3-aminopropyl(methyl)phosphinic acid

3-{[(1R)-isobutanoyloxyisobutoxy]carbonylamino}propyl methylphosphinic acid

3-{[(1R)-isobutanoyloxyisobutoxy]carbonylamino}propyl methylphosphinic acid

Conditions
ConditionsYield
With water In tetrahydrofuran at 18 - 20℃; for 4h;
1-[[[(2,5-dioxopyrrolidin-1-yl)oxy]carbonyl]oxy]ethyl 2-methylpropanoate
860035-10-5

1-[[[(2,5-dioxopyrrolidin-1-yl)oxy]carbonyl]oxy]ethyl 2-methylpropanoate

3-aminopropyl(methyl)phosphinic acid
127729-35-5

3-aminopropyl(methyl)phosphinic acid

3-{[1-isobutanoyloxyethoxy]carbonylamino}propyl methylphosphinic acid

3-{[1-isobutanoyloxyethoxy]carbonylamino}propyl methylphosphinic acid

Conditions
ConditionsYield
In acetonitrile at 20℃; for 16h;

127729-35-5Upstream product

127729-35-5Downstream Products

127729-35-5Relevant articles and documents

Use of GABA and GABAB agonists

-

, (2008/06/13)

The present invention provides methods of stimulating tissue growth, including islet cell growth, by administering GABA or a GABA agonist to act on GABAB receptors and GABAB-like receptors to activate cell replication.

Substituted aminoalkylphosphinic acids

-

, (2008/06/13)

P-substituted aminoalkylphosphinic acids of the formula STR1 wherein R denotes an optionally fluorinated methyl group, R1 denotes hydrogen, lower alkyl, lower alkoxy, hydroxy, halogen or a fluorinated methyl group and R2 and R3 denote hydrogen or R2 denotes hydroxy, lower alkoxy or halogen and R3 is hydrogen or R2 and R3 together represent an oxo group, and their pharmaceutically acceptable salts are active as GABAB- agonists and can be used in the treatment of spinal spasticity, multiple sclerosis and cerebral palsy, trigeminus neuralgia, drug withdrawal syndromes and/or conditions of pain. They can be manufactured by methods known per se and suitable such methods are described.

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