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t-butyl β-isopropyl-β-phenylglycidate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 21297-92-7 Structure
  • Basic information

    1. Product Name: t-butyl β-isopropyl-β-phenylglycidate
    2. Synonyms: t-butyl β-isopropyl-β-phenylglycidate
    3. CAS NO:21297-92-7
    4. Molecular Formula:
    5. Molecular Weight: 262.349
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 21297-92-7.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: t-butyl β-isopropyl-β-phenylglycidate(CAS DataBase Reference)
    10. NIST Chemistry Reference: t-butyl β-isopropyl-β-phenylglycidate(21297-92-7)
    11. EPA Substance Registry System: t-butyl β-isopropyl-β-phenylglycidate(21297-92-7)
  • 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: 21297-92-7(Hazardous Substances Data)

21297-92-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21297-92-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,2,9 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 21297-92:
(7*2)+(6*1)+(5*2)+(4*9)+(3*7)+(2*9)+(1*2)=107
107 % 10 = 7
So 21297-92-7 is a valid CAS Registry Number.

21297-92-7Downstream Products

21297-92-7Relevant articles and documents

A Comparative Study of Pyrolysis and Decarboxylation of β-Substituted t-Butyl Glycidates

Bansal, R.K.,Sethi, K.,Jain, S.K.

, p. 121 - 124 (2007/10/02)

A series of t-butyl glycidates (Ia-i) have been prepared by Darzens condensation of carbonyl compounds with t-butyl chloroacetate in the presence of potassium t-butoxide.The pyrolysis of these esters (I) and the decarboxylation of potassium salts of the corresponding acids result in the same higher aldehydes (II) though in varying proportions.The latter procedure has, however, been found to be superiour in all the cases.Structural assignments of I and II are based on elemental analyses and spectral data (IR, PMR).Resolution of cis- and trans-isomers of I has been achieved in three cases.

Mass Spectrometric Studies of t-Butyl β-Phenylglycidates

Bansal, R. K.,Sethi, K.,Bachelor, F. W.

, p. 515 - 517 (2007/10/02)

The effect of β-substitution on the fragmentation pattern of t-butyl β-phenylglycidates (I-VII) has been elucidated.Unlike ethyl β-phenylglycidates it has been found that the migration of t-butoxy group does not take place in the esters (I-VII).Structures

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