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Aminooxyacetic Acid, Hydrochloride Salt Discontinued See: C178730 is a chemical compound that has been discontinued and is now identified as a different product with the code C178730. It is used in the synthesis of pharmaceuticals and is known for its ability to inhibit the enzymatic activity of pyridoxal phosphate-dependent enzymes. In its hydrochloride salt form, it is generally used in research and laboratory settings for its unique chemical properties.

20295-82-3

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20295-82-3 Usage

Uses

Used in Pharmaceutical Synthesis:
Aminooxyacetic Acid, Hydrochloride Salt Discontinued See: C178730 is used as a key intermediate in the synthesis of various pharmaceutical compounds due to its ability to inhibit the enzymatic activity of pyridoxal phosphate-dependent enzymes.
Used in Research and Laboratory Settings:
Aminooxyacetic Acid, Hydrochloride Salt Discontinued See: C178730 is used in research and laboratory settings to study its unique chemical properties and potential applications in various fields.
Note: Since the compound has been discontinued and is no longer commercially available, it can still be obtained under the new product code C178730.

Check Digit Verification of cas no

The CAS Registry Mumber 20295-82-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,2,9 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 20295-82:
(7*2)+(6*0)+(5*2)+(4*9)+(3*5)+(2*8)+(1*2)=93
93 % 10 = 3
So 20295-82-3 is a valid CAS Registry Number.

20295-82-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (aminooxy)acetic acid hemihydrochloride

1.2 Other means of identification

Product number -
Other names Aminooxyacetic Acid, Hydrochloride Salt

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:20295-82-3 SDS

20295-82-3Relevant academic research and scientific papers

PROCESS FOR PRODUCTION OF O-SUBSTITUTED HYDROXYLAMINES

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Page/Page column 4, (2008/06/13)

[Purpose] The purpose of the present invention is to provide a method for the production of O-substituted hydroxylamine compounds at a high yield by using industrially available starting material. [Solution method] Method for the production of O-substituted hydroxylamine compounds comprising a process of obtaining O-substituted hydroxylamine disulfonic acid alkali metal salts by reacting hydroxylamine disulfonic acid alkali metal salts with halides exemplified by alkylating agents (RX), and a process of hydrogenating the obtained O-substituted hydroxylamine disulfonic acid alkali metal salt.

Aminooxyamide tricyclic inhibitors of farnesyl-protein transferase

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, (2008/06/13)

Novel aminooxyamide tricyclic compounds and pharmaceutical compositions are disclosed which are inhibitors of the enzyme, farnesyl protein transferase. Also disclosed is a method of inhibiting Ras function and therefore inhibiting the abnormal growth of cells. The method comprises administering the novel aminooxyamide tricyclic compound to a biological system. In particular, the method inhibits the abnormal growth of cells in a mammals such as a human.

Process for producing aminooxyacetic acid salts

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, (2008/06/13)

A process for producing an aminooxyacetic acid salt comprises reacting benzhydroxamic acid of formula: STR1 (where R1 is a hydrogen atom, an alkyl group, an alkoxy group or a halogen atom) with a halogenoacetic acid of formula: (where X is an iodine, bromine or chlorine atom) in the presence of a metal hydroxide or a metal carbonate to form benzamidooxyacetic acid of formula (IV): STR2 and thereafter hydrolyzing the benzamidooxyacetic acid in the presence of a mineral acid to obtain an aminooxyacetic acid salt of formula:

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