2-AMINO-2-(4-METHYLPHENYL)ACETIC ACID

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Company Name: Capot Chemical Co.,Ltd.
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Products Intro: Product Name:DL-4-Methylphenylglycine
CAS:13227-01-5
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
Company Name: Changzhou Ansciep Chemical Co., Ltd.
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Products Intro: Product Name:DL-4-methylphenylglycine
CAS:13227-01-5
Purity:98% Package:100g, 500g, 1kg, 25kg, 50kg, 200kg Remarks:Good quality; Large stock; Hot sale
Company Name: Alchem Pharmtech,Inc.
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Products Intro: Product Name:2-Amino-2-(p-tolyl)acetic acid
CAS:13227-01-5
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-20701
Company Name: Wuhan Chemwish Technology Co., Ltd
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Products Intro: Product Name:DL-4-Methylphenylglycine
CAS:13227-01-5
Purity:0.98 Package:1g;5g;25g;100;500g
Company Name: CONIER CHEM AND PHARMA LIMITED
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Products Intro: Product Name:2-AMINO-2-(4-METHYLPHENYL)ACETIC ACID
CAS:13227-01-5
Purity:99% Package:1kg

2-AMINO-2-(4-METHYLPHENYL)ACETIC ACID manufacturers
2-AMINO-2-(4-METHYLPHENYL)ACETIC ACID Basic information
Product Name:2-AMINO-2-(4-METHYLPHENYL)ACETIC ACID
Synonyms:Benzeneaceticacid,α-aMino-4-Methyl-;2-amino-2-p-tolylacetic acid;4-Methylphenyl glycin;2-AMINO-2-(4-METHYLPHENYL)ACETIC ACID;4-METHYLPHENYL GLYCINE;AMINO-P-TOLYL-ACETIC ACID;DL-4-METHYLPHENYLGLYCINE;RARECHEM AK ML 0528
CAS:13227-01-5
MF:C9H11NO2
MW:165.19
EINECS:
Product Categories:pharmacetical
Mol File:13227-01-5.mol
2-AMINO-2-(4-METHYLPHENYL)ACETIC ACID Structure
2-AMINO-2-(4-METHYLPHENYL)ACETIC ACID Chemical Properties
Melting point 256-257°
Boiling point 306.8±30.0 °C(Predicted)
density 1.200±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility Acetonitrile: Slightly soluble: 0.1-1 mg/ml
form solid
pka2.03±0.10(Predicted)
color White
CAS DataBase Reference13227-01-5(CAS DataBase Reference)
Safety Information
HazardClass IRRITANT
HS Code 2922498590
MSDS Information
2-AMINO-2-(4-METHYLPHENYL)ACETIC ACID Usage And Synthesis
Uses2-Amino-2-(p-tolyl)acetic acid is used for optimizing azide skeleton, and is the intermediate in the synthesis of 1,3, 4-thiadiazole compounds. 1,3,4-thiadiazole compounds exhibit potential anti-cancer activity, and inhibit glutaminase (GLSI)[1][2].
References[1] Kalie A M, et al. Cytosolic Delivery of Proteins by Bioreversible Esterification. JAmChem. 2017. 139(41):14396–14398.
[2] Finlay MRV, et al. Preparation of 1,3,4-thiadiazole compounds and their use in treating cancer: World Intellectual Property Organization, WO2017093301[P]. 2017-06-08.
[3] JERZY ZOŃ  Roman G  Nikolaus Amrhein. Inhibitors of phenylalanine ammonia-lyase: 1-aminobenzylphosphonic acids substituted in the benzene ring[J]. Phytochemistry, 2002, 59 1: Pages 9-21. DOI: 10.1016/s0031-9422(01)00425-3
Tag:2-AMINO-2-(4-METHYLPHENYL)ACETIC ACID(13227-01-5) Related Product Information
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