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138714-61-1

BETA-OXO-4-DIMETHYLAMINO-BENZENEPROPANOIC ACID 1,1-DIMETHYLETHYL ESTER is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 138714-61-1 Structure

  • Basic information

    1. Product Name: BETA-OXO-4-DIMETHYLAMINO-BENZENEPROPANOIC ACID 1,1-DIMETHYLETHYL ESTER
    2. Synonyms: BETA-OXO-4-DIMETHYLAMINO-BENZENEPROPANOIC ACID 1,1-DIMETHYLETHYL ESTER;tert-Butyl b-oxo-4-dimethylaminobenzenepropanoate
    3. CAS NO:138714-61-1
    4. Molecular Formula: C15H21NO3
    5. Molecular Weight: 263.335
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 138714-61-1.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: BETA-OXO-4-DIMETHYLAMINO-BENZENEPROPANOIC ACID 1,1-DIMETHYLETHYL ESTER(CAS DataBase Reference)
    10. NIST Chemistry Reference: BETA-OXO-4-DIMETHYLAMINO-BENZENEPROPANOIC ACID 1,1-DIMETHYLETHYL ESTER(138714-61-1)
    11. EPA Substance Registry System: BETA-OXO-4-DIMETHYLAMINO-BENZENEPROPANOIC ACID 1,1-DIMETHYLETHYL ESTER(138714-61-1)

  • 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: 138714-61-1(Hazardous Substances Data)

138714-61-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138714-61-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,7,1 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 138714-61:
(8*1)+(7*3)+(6*8)+(5*7)+(4*1)+(3*4)+(2*6)+(1*1)=141
141 % 10 = 1
So 138714-61-1 is a valid CAS Registry Number.

138714-61-1Relevant articles and documents

SYNTHESIS AND CHARACTERIZATION OF PYRROLINONECARBOXYLATES FORMED BY REACTION OF VICINAL TRICARBONYL DERIVATIVES WITH ALDEHYDE SCHIFF BASES

Wasserman, Harry H.,Ennis, David S.,Vu, Chi B.,Schulte, Gayle,Munk, Morton E.,et al.

, p. 975 - 995 (2007/10/02)

A series of vicinal tricarbonyl derivatives undergo reaction with aldehyde Schiff bases forming pyrrolinone derivatives by benzilic acid-related rearrangements.The structures were established by X-ray analyses and, independently by the SESAMI NMR-based computer program.

BENZILIC ACID REARRANGEMENTS IN THE REACTIONS OF ARYL VICINAL TRICARBONYL DERIVATIVES WITH ALDEHYDE SCHIFF BASES

Wasserman, Harry H.,Ennis, David S.,Vu, Chi B.,Schulte, Gayle K.

, p. 6039 - 6042 (2007/10/02)

Reactions of aryl and hetero vicinal tricarbonyl derivatives with aldehyde Schiff bases of the general structure RCH2CHO lead to pyrrolinone derivatives by benzilic acid-related rearrangements, driven, most probably, by iminium ion intermediates.

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