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alpha-amino-3-(hydroxy)-5-methyl-4-isoxazoleacetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77006-27-0

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77006-27-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77006-27-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,0,0 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 77006-27:
(7*7)+(6*7)+(5*0)+(4*0)+(3*6)+(2*2)+(1*7)=120
120 % 10 = 0
So 77006-27-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H8N2O4/c1-2-3(4(7)6(10)11)5(9)8-12-2/h4H,7H2,1H3,(H,8,9)(H,10,11)

77006-27-0SDS

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 2-amino-2-(5-methyl-3-oxo-1,2-oxazol-4-yl)acetic acid

1.2 Other means of identification

Product number -
Other names Amaa acid

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:77006-27-0 SDS

77006-27-0Downstream Products

77006-27-0Relevant academic research and scientific papers

Synthesis of tritiated (RS)-2-amino-2-(3-hydroxy-5-methylisoxazol-4-yl)acetic acid (AMAA), a potent and selective NMDA agonist

Johansen, Tommy N.,Balasubramanian, Venkataraman,Madsen, Ulf,Ferkany, John W.,Krogsgaard-Larsen, Povl

, p. 915 - 922 (2007/10/03)

(RS)-2-Amino-2-(3-hydroxy-5-methylisoxazol-4-yl)acetic acid (AMAA) is a potent and selective agonist at the NMDA subgroup of excitatory amino acid receptors. To probe its interaction with these receptors we have developed a synthesis of [3H]AMAA. Bromination of a protected form of AMAA with NBS followed by hydrogenolysis with tritium gas in the presence of Pd/C and subsequent deprotection gave [3H]AMAA with a specific activity of 25 Ci/mmol. Attempts to develop a receptor binding assay based on rat brain homogenates and using [3H]AMAA as radioligand for the NMDA receptors have not been successful.

N-methyl-D-aspartic acid receptor agonists: Resolution, absolute stereochemistry, and pharmacology of the enantiomers of 2-amino-2-(3-hydroxy-5-methyl-4-isoxazolyl)acetic acid

Madsen, Ulf,Frydenvang, Karla,Ebert, Bjarke,Johansen, Tommy N.,Brehm, Lotte,Krogsgaard-Larsen, Povl

, p. 183 - 190 (2007/10/03)

(R,S)-2-Amino-2-(3-hydroxy-5-methyl-4-isoxazolyl)acetic acid [(R,S)-AMAA, 4] is a potent and selective agonist at the N-methyl-D-aspartic acid (NMDA) subtype of excitatory amino acid receptors. Using the Ugi "four-component condensation" method, the two d

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