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1531585-26-8

benzyl 2-cyclopropyl-2-methylpropanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1531585-26-8 Structure

  • Basic information

    1. Product Name: benzyl 2-cyclopropyl-2-methylpropanoate
    2. Synonyms: benzyl 2-cyclopropyl-2-methylpropanoate
    3. CAS NO:1531585-26-8
    4. Molecular Formula:
    5. Molecular Weight: 204.269
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1531585-26-8.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: benzyl 2-cyclopropyl-2-methylpropanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: benzyl 2-cyclopropyl-2-methylpropanoate(1531585-26-8)
    11. EPA Substance Registry System: benzyl 2-cyclopropyl-2-methylpropanoate(1531585-26-8)

  • 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: 1531585-26-8(Hazardous Substances Data)

1531585-26-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1531585-26-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,3,1,5,8 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1531585-26:
(9*1)+(8*5)+(7*3)+(6*1)+(5*5)+(4*8)+(3*5)+(2*2)+(1*6)=158
158 % 10 = 8
So 1531585-26-8 is a valid CAS Registry Number.

1531585-26-8Downstream Products

1531585-26-8Relevant articles and documents

FLUOROALKYL-OXADIAZOLES AND USES THEREOF

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Paragraph 00222-00223, (2021/06/26)

Provided herein are compounds identified as inhibitors of HDAC6 activity that can be used to treat various diseases and disorders.

COMBINATIONS OF HEPATITIS C VIRUS INHIBITORS

-

, (2015/02/02)

The present disclosure is generally directed to antiviral compounds, and more specifically directed to combinations of compounds which can inhibit the function of the NS5A protein encoded by Hepatitis C virus (HCV), compositions comprising such combinations, and methods for inhibiting the function of the NS5A protein.

Direct carboxylation of allylic halides with carbon dioxide in the presence of indium

Miao, Bukeyan,Ma, Shengming

supporting information, p. 3285 - 3287 (2014/03/21)

A highly regioselective indium-mediated allylation of carbon dioxide starting from simple allylic halides (X = I, Br, Cl) has been developed. No transition metal catalyst is needed and an inert atmosphere is not necessary. The reaction tolerates a wide range of synthetically attractive functional groups with a very high branched regioselectivity. The Royal Society of Chemistry 2014.

Synthesis of the spiroacetal core of the cephalosporolide family of natural products

Finch, Orla C.,Furkert, Daniel P.,Brimble, Margaret A.

, p. 590 - 596 (2014/02/14)

The synthesis of four possible stereoisomers of the spiroacetal core of the natural products cephalosporolides H and I and penisporolides A and B is described. The key steps involve the use of Sharpless asymmetric dihydroxylation to install the desired stereochemistry of the γ-lactone ring and an oxidative radical cyclisation to form the spiroacetal ring system.

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