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132660-03-8

2-<5'-(Dimethylamino)-4',4'-dimethyl-4'H-imidazol-2'-yl>-2-phenylbutanamid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 132660-03-8 Structure

  • Basic information

    1. Product Name: 2-<5'-(Dimethylamino)-4',4'-dimethyl-4'H-imidazol-2'-yl>-2-phenylbutanamid
    2. Synonyms: 2-<5'-(Dimethylamino)-4',4'-dimethyl-4'H-imidazol-2'-yl>-2-phenylbutanamid
    3. CAS NO:132660-03-8
    4. Molecular Formula:
    5. Molecular Weight: 300.404
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 132660-03-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-<5'-(Dimethylamino)-4',4'-dimethyl-4'H-imidazol-2'-yl>-2-phenylbutanamid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-<5'-(Dimethylamino)-4',4'-dimethyl-4'H-imidazol-2'-yl>-2-phenylbutanamid(132660-03-8)
    11. EPA Substance Registry System: 2-<5'-(Dimethylamino)-4',4'-dimethyl-4'H-imidazol-2'-yl>-2-phenylbutanamid(132660-03-8)

  • 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: 132660-03-8(Hazardous Substances Data)

132660-03-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132660-03-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,6,6 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 132660-03:
(8*1)+(7*3)+(6*2)+(5*6)+(4*6)+(3*0)+(2*0)+(1*3)=98
98 % 10 = 8
So 132660-03-8 is a valid CAS Registry Number.

132660-03-8Relevant articles and documents

Reactions of 3-(Dimethylamino)-2,2-dimethyl-2H-azirines with Barbituric-Acid Derivatives

Schlaepfer-Daehler, Marlise,Heimgartner, Heinz

, p. 2275 - 2286 (2007/10/02)

The reaction of 3-(dimethylamino)-2,2-dimethyl-2H-azirine (1) and 5,5-disubstituted barbituric acids 5 in i-PrOH at ca. 70 deg gives 2-alkanamides of type 6 in good yields (Scheme 1).The formation of 6 proceeds with loss of CO2; various reaction mechanisms with a zwitterionic 1:1 adduct B as common intermediate are discussed (Schemes 2 and 5).Thermolysis of product 6 leads to 2-alkyl-5-(dimethylamino)-4,4-dimethyl-4H-imidazoles 8 or the tautomeric 2-alkylidene derivatives 8'via elimination of HNCO (Scheme 3).The latter undergoes trimerization to give 1,3,5-triazine-2,4,6-trione.No reaction is observed with 1,5,5-trisubstituted barbiturates and 1 in refluxing i-PrOH, but an N-alkylation of the barbiturate occurs in the presence of morpholine (Scheme 4).This astonishing reaction is explained by a mechanism via formation of the 2-alkoxy-2-(dimethylamino)aziridinium ion H which undergoes ring opening to give the O-alkylated 2-amino-N1,N1-dimethylisobutyramide I as alkylating reagent (Scheme 4).

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