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CAS

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305857-90-3

4-acetylphenyl 4-bromobenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 305857-90-3 Structure

  • Basic information

    1. Product Name: 4-acetylphenyl 4-bromobenzoate
    2. Synonyms: 4-acetylphenyl 4-bromobenzoate;benzoic acid, 4-bromo-, 4-acetylphenyl ester;(4-ethanoylphenyl) 4-bromobenzoate;4-bromobenzoic acid (4-acetylphenyl) ester;A0840/0039414;AK-918/40022414;EU-0051010;ZINC00060378
    3. CAS NO:305857-90-3
    4. Molecular Formula: C15H11BrO3
    5. Molecular Weight: 319.15004
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 305857-90-3.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: 4-acetylphenyl 4-bromobenzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-acetylphenyl 4-bromobenzoate(305857-90-3)
    11. EPA Substance Registry System: 4-acetylphenyl 4-bromobenzoate(305857-90-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 305857-90-3(Hazardous Substances Data)

305857-90-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 305857-90-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,5,8,5 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 305857-90:
(8*3)+(7*0)+(6*5)+(5*8)+(4*5)+(3*7)+(2*9)+(1*0)=153
153 % 10 = 3
So 305857-90-3 is a valid CAS Registry Number.

305857-90-3Downstream Products

305857-90-3Relevant articles and documents

Radical Carbonyl Umpolung Arylation via Dual Nickel Catalysis

Huang, Huan-Ming,Bellotti, Peter,Erchinger, Johannes E.,Paulisch, Tiffany O.,Glorius, Frank

supporting information, p. 1899 - 1909 (2022/02/01)

The formation of carbon-carbon bonds lies at the heart of synthetic organic chemistry and is widely applied to construct complex drugs, polymers, and materials. Despite its importance, catalytic carbonyl arylation remains comparatively underdeveloped, due

Transesterification for synthesis of carboxylates using aldehydes as acyl donors via C-H and C-O bond activations

Bao, Yong-Sheng,Chen, Chao-Yue,Huang, Zhi-Zhen

, p. 8344 - 8349,6 (2020/10/15)

A new type of transesterification between aryl, heteroaryl, alkyl N-heteroarene-2-carboxylates and various aldehydes by C-H and C-O bond activations has been developed for the synthesis of versatile carboxylates. A possible mechanism containing oxidative addition of acyl-O bond in parent ester and radical cleavage of sp2 C-H bond in aldehyde is proposed.

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