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115377-63-4

1H-Imidazole-5-carboxamide,4-amino-1-ethyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 115377-63-4 Structure

  • Basic information

    1. Product Name: 1H-Imidazole-5-carboxamide,4-amino-1-ethyl-(9CI)
    2. Synonyms: 1H-Imidazole-5-carboxamide,4-amino-1-ethyl-(9CI);5-Amino-3-ethyl-3H-imidazole-4-carboxylic acid amide
    3. CAS NO:115377-63-4
    4. Molecular Formula: C6H10N4O
    5. Molecular Weight: 154.1698
    6. EINECS: N/A
    7. Product Categories: AMIDE
    8. Mol File: 115377-63-4.mol

  • Chemical Properties

    1. Melting Point: 133-134 °C(Solv: ethyl acetate (141-78-6))
    2. Boiling Point: 427.4±25.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.45±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 15.08±0.50(Predicted)
    10. CAS DataBase Reference: 1H-Imidazole-5-carboxamide,4-amino-1-ethyl-(9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1H-Imidazole-5-carboxamide,4-amino-1-ethyl-(9CI)(115377-63-4)
    12. EPA Substance Registry System: 1H-Imidazole-5-carboxamide,4-amino-1-ethyl-(9CI)(115377-63-4)

  • 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: 115377-63-4(Hazardous Substances Data)

115377-63-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115377-63-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,3,7 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 115377-63:
(8*1)+(7*1)+(6*5)+(5*3)+(4*7)+(3*7)+(2*6)+(1*3)=124
124 % 10 = 4
So 115377-63-4 is a valid CAS Registry Number.

115377-63-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-amino-1-ethyl-1H-imidazole-5-carboxamide

1.2 Other means of identification

Product number -
Other names 5-Amino-3-ethyl-3H-imidazole-4-carboxylic acid amide

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:115377-63-4 SDS

115377-63-4Downstream Products

115377-63-4Relevant articles and documents

Purines. XXX. Ring Fission of 3,7-Dialkyladenines by Alkaline Hydrolysis

Fujii, Tozo,Saito, Tohru,Inoue, Isao,Kumazawa, Yukinari,Tamura, Katsumi

, p. 107 - 117 (2007/10/02)

On treatment with boiling 1 N aqueous NaOH for 2 h, 3,7-dialkyladenine salts (7: R1, R2= Me, Et, or PhCH2; X= Br, I, or ClO4) gave 1-alkyl-4-(N-alkylamino)-1H-imidazole-5-carboxamides (8), 1-alkyl-4-amino-1H-imidazole-5-carboxamides (11), and N6,7-dialkyladenines (14) in 33-59 percent, 2-10 percent, and 2-5 percent yields, respectively.Under slightly milder reaction conditions, 3,7-dimethyladenine hydriodide (7a: X= I) afforded 1-methyl-4-(N-methylamino)-1H-imidazole-5-carboxamide (8a) together with 3,7-dimethylhypoxanthine (2a) as a by-product; 7-benzyl-3-methyladenine hydrobromide (7c: X= Br) furnished a small amount of 1-benzyl-4-(N-methylamino)-1H-imidazole-5-carboxamidine (5c) besides 1-benzyl-4-(N-methylamino)-1H-imidazole-5-carboxamide (8c), 1-benzyl-4-amino-1H-imidazole-5-carboxamide (11c), and 7-benzyl-N6-methyladenine (14c).These results are best interpreted in terms of pathways involving hydrolytic deamination, ring fission in the pyrimidine and imidazole moieties, cyclization, and Dimroth rearrangement.The instability of 7a (X= I) in aqueous alkali was compared with that of the four possible Nx,9-dimethyl isomers, and the relative ease with which the adenine ring underwent hydrolytic ring fission was found to decrease in the order 3,9- (17) >7,9- (18) >1,9- (19) >3,7- (7a) >>N6,9-dimethyl isomer (20).Keywords - 3,7-dialkyladenine alkaline hydrolysis; ring fission; deamination; rearrangement; 1-alkyl-4-(N-alkylamino)-1H-imidazole-5-carboxamide; 1-alkyl-4-amino-1H-imidazole-5-carboxamide; N6,7-dialkyladenine

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