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1380086-03-2

C11H16O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1380086-03-2 Structure

  • Basic information

    1. Product Name: C11H16O2
    2. Synonyms: C11H16O2
    3. CAS NO:1380086-03-2
    4. Molecular Formula:
    5. Molecular Weight: 180.247
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1380086-03-2.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: C11H16O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C11H16O2(1380086-03-2)
    11. EPA Substance Registry System: C11H16O2(1380086-03-2)

  • 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: 1380086-03-2(Hazardous Substances Data)

1380086-03-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1380086-03-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,0,0,8 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1380086-03:
(9*1)+(8*3)+(7*8)+(6*0)+(5*0)+(4*8)+(3*6)+(2*0)+(1*3)=142
142 % 10 = 2
So 1380086-03-2 is a valid CAS Registry Number.

1380086-03-2Upstream product

1380086-03-2Relevant articles and documents

P-Methylbenzyl Group: Oxidative Removal and Orthogonal Alcohol Deprotection

Ikeuchi, Kazutada,Murasawa, Kentaro,Ohara, Kenya,Yamada, Hidetoshi

, p. 6638 - 6642 (2019)

We describe the practical removal of p-methylbenzyl (MBn) protections of alcohols by treatment with 2,3-dichloro-5,6-dicyano-p-benzoquinone. When a molecule bears benzyl and MBn groups, the oxidant selectively removes the latter groups. Further, the MBn groups tolerate ceric ammonium nitrate, resulting in chemoselective removal of the p-methoxybenzyl group in the presence of the MBn groups. These orthogonal alcohol deprotections would provide novel synthetic strategies of organic compounds.

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