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ethyl 2-amino-2-cyanoacetate oxalate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 150464-08-7 Structure
  • Basic information

    1. Product Name: ethyl 2-amino-2-cyanoacetate oxalate
    2. Synonyms: ethyl 2-amino-2-cyanoacetate oxalate
    3. CAS NO:150464-08-7
    4. Molecular Formula: C7H10N2O6
    5. Molecular Weight: 218.17
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 150464-08-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: ethyl 2-amino-2-cyanoacetate oxalate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 2-amino-2-cyanoacetate oxalate(150464-08-7)
    11. EPA Substance Registry System: ethyl 2-amino-2-cyanoacetate oxalate(150464-08-7)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 150464-08-7(Hazardous Substances Data)

150464-08-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 150464-08-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,4,6 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 150464-08:
(8*1)+(7*5)+(6*0)+(5*4)+(4*6)+(3*4)+(2*0)+(1*8)=107
107 % 10 = 7
So 150464-08-7 is a valid CAS Registry Number.

150464-08-7Relevant articles and documents

Preparative route to 2-ethoxycarbonylimidazole-4-phosphonate and diethyl imidazole-2,4-dicarboxylate

Vuilhorgne, Marc,Malpart, Joel,Mutti, Stephane,Mignani, Serge

, p. 159 - 162 (2007/10/03)

Practical synthesis of 2-ethoxycarbonylimidazole-4-phosphonate (1a) and diethyl imidazole-2,4-dicarboxylate (1b) are described.

Purines, Pyrimidines, and Imidazoles. Part 53. Synthesis of Some 5-Halogeno-analogues of Metiamide and Cimetidine

Brown, Tom,Shaw, Gordon,Durant, Graham J.

, p. 2310 - 2315 (2007/10/02)

Ethyl 5-chloroimidazole-4-carboxylate has been prepared by diazotisation of ethyl 5-amino-1-(di-O-isopropylidene-α- or α,β-D-mannofuranosyl)imidazole-4-carboxylate, reaction of the diazonium salt with copper(I) chloride and removal of the 1-substituent with hydrochloric acid, or by similar conversion of ethyl 5-amino-1-t-butylimidazole-4-carboxylate to ethyl 1-t-butyl-5-chloroimidazole-4-carboxylate, and removal of the t-butyl group with hydrogen bromide.Ethyl 5-fluoroimidazole-4-carboxylate has been prepared from ethyl 5-amino-1-t-butylimidazole-4-carboxylate by diazotisation and photolysis in the presence of tetrafluoroboric acid.Ethyl 5-chloroimidazole-4-carboxylate and ethyl 5-fluoroimidazole-4-carboxylate have been converted into the corresponding alcohols by reaction with lithium aluminium hydride. 5-Chloro-4-(hydroxymethyl)imidazole has also been prepared by electrolysis of 5-chloroimidazole-4-carboxylic acid at mercury cathode. 5-Chloroimidazole has been converted into the 5-chloroimidazolyl analogues of metiamide and cimetidine by a sequence of reactions, and 5-fluoroimidazole has been similarly converted into the 5-fluoro-analogue of metiamide.The metiamide and cimetidine analogues were found to be histamine H2-receptor antagonists.

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