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Detail of "16115-80-3"

  • CAS Number:
  • 16115-80-3
  • Name:
  • Propanedioic acid,2-amino-, 1,3-dimethyl ester, hydrochloride (1:1)

  • Superlist Name:
  • Dimethyl aminomalonate hydrochloride
  • Molecular Structure:
  • Formula:
  • C5H10ClNO4
  • Molecular Weight:
  • 183.5902
  • Synonyms:
  • Malonicacid, amino-, dimethyl ester, hydrochloride (6CI,8CI);Propanedioic acid, amino-,dimethyl ester, hydrochloride (9CI);Aminomalonic acid dimethyl esterhydrochloride;Dimethyl aminomalonate hydrochloride;
  • EINECS:
  • 240-284-5
  • Density:
  • 1.205g/cm3
  • Melting Point:
  • 160 °C (dec.)(lit.)
  • Boiling Point:
  • 155.7 °C at 760 mmHg
  • Flash Point:
  • 33.2 °C
  • Appearance:
  • light yellow crystals or crystalline powder
  • Hazard Symbols:
  • IrritantXi
  • Risk Codes:
  • 36/37/38
  • Safety:
  • 26-36 Details

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CAS No.16115-80-3 Dimethyl aminomalonate hydrochloride

Supplier:Ruiyuan Group Limited [ China (Mainland)]

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CAS No.16115-80-3 Dimethyl aminomalonate hydrochloride

Assay:98%

Supplier:Shanghai Nava Chemical [ China (Mainland)]

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Address:RM411-415 Bldg.2 No. 2715 Longwu Rd.,Xuhui Dist,Shanghai China

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CAS No.16115-80-3 Dimethyl aminomalonate hydrochloride

2-Aminomalonic acid dimethyl ester hydrochloride

Supplier:Synthon Chemicals GmbH & Co. KG [ Germany]

610Integral
610

Tel:+49 3494 636983

Address:Chemiepark Bitterfeld-Wolfen, Areal A, Werkstattstrasse 10

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Reference

Metabolic products of microorganisms
Metabolic products of microorganisms. Part 159. The aromatic amino acid constituents of echinocandin B: 3,4-dihydroxyhomotyrosine. Keller-Schierlein, Walter; Widmer, Joerg (Org.-Chem. Lab.Some commonly used reagents like 16115-80-3 and 61172-70-1 are used in this experiment., ETH, Zurich, Switz.). Helv. Chim. Acta, 59(6), 2021-31 (German) 1976. CODEN: HCACAV. DOCUMENT TYPE: Journal CA Section: 34 (Synthesis of Amino Acids, Peptides, and Proteins) Section cross-reference(s): 10 4-HOC6H4CH(OH)CH(OH)CH(NH2)CO2H (I) is a constituent of the antifungal antibiotic echinocandin B. When tetrahydro-echinocandin B (II) was treated with CF3CO2H and MeOH, H-Thr-Hyp-NHCH(CH2COC6H4OH-4)CO2Me was obtained. Periodate degrdn. of II gave 4-HOC6H4CHO, and I was obtained from mild acid treatment of II. 4-AcOC6H4CH2COCH2NHAc, which has been obtained from the acid hydrolysis of echinocandin B, was prepd. .
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