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1185836-99-0

2-CyclopropylMethoxy-5-Methylphenylboronic acid pinacol ester is a chemical compound that is an ester derivative of boronic acid, featuring a cyclopropylmethoxy and methylphenyl group. It is a versatile and important compound in the field of organic chemistry and drug development.

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  • 1185836-99-0 Structure

  • Basic information

    1. Product Name: 2-CyclopropylMethoxy-5-Methylphenylboronic acid pinacol ester
    2. Synonyms: 2-CyclopropylMethoxy-5-Methylphenylboronic acid pinacol ester;2-(2-Cyclopropylmethoxy-5-methylphenyl)-4,4,5,5-tetramethyl[1,3,2]dioxaborolane
    3. CAS NO:1185836-99-0
    4. Molecular Formula: C17H27BO4
    5. Molecular Weight: 306.20488
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1185836-99-0.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: 2-CyclopropylMethoxy-5-Methylphenylboronic acid pinacol ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-CyclopropylMethoxy-5-Methylphenylboronic acid pinacol ester(1185836-99-0)
    11. EPA Substance Registry System: 2-CyclopropylMethoxy-5-Methylphenylboronic acid pinacol ester(1185836-99-0)

  • 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: 1185836-99-0(Hazardous Substances Data)

1185836-99-0 Usage

Uses

Used in Organic Synthesis:
2-CyclopropylMethoxy-5-Methylphenylboronic acid pinacol ester is used as a reagent in organic synthesis for its ability to form carbon-carbon bonds through Suzuki-Miyaura cross-coupling reactions. This is important in the synthesis of complex organic molecules and pharmaceuticals.
Used in Drug Discovery:
2-CyclopropylMethoxy-5-Methylphenylboronic acid pinacol ester is used as a valuable reagent in drug discovery due to its potential applications in the development of new pharmaceuticals. The pinacol ester group increases the stability and solubility of the boronic acid, making it suitable for a variety of chemical reactions in the synthesis of bioactive compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 1185836-99-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,5,8,3 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1185836-99:
(9*1)+(8*1)+(7*8)+(6*5)+(5*8)+(4*3)+(3*6)+(2*9)+(1*9)=200
200 % 10 = 0
So 1185836-99-0 is a valid CAS Registry Number.

1185836-99-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Cyclopropylmethoxy-5-methylphenylboronic acid pinacol ester

1.2 Other means of identification

Product number -
Other names 2-[2-(cyclopropylmethoxy)-5-methylphenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1185836-99-0 SDS

1185836-99-0Upstream product

1185836-99-0Downstream Products

1185836-99-0Relevant articles and documents

METHYLPYRROLOPYRIMIDINECARBOXAMIDES

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Page/Page column 107, (2012/06/18)

The compounds of Formula (I), wherein R1, R2, R21, R22, R23, R24, Y and R3 have the meanings as given in the description, the salts thereof, the stereoisomers of the compounds and the salts thereof are effective inhibitors of the type 5 phosphodiesterase.

METHYLPYRROLOPYRIMIDINECARBOXAMIDES

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Page/Page column 173, (2011/04/14)

The compounds of formula (I) wherein R1, R2, R21, R22, R23, R24, Y and R3 have the meanings as given in the description, the salts thereof, and the stereoisomers of the compounds and the salts thereof are effective inhibitors of the type 5 phosphodiestera

METHYLPYRROLOPYRIDINECARBOXAMIDES

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Page/Page column 89, (2011/04/14)

The compounds of formula (I) wherein R1, R21, R22, R23, R24, Y and R3 have the meanings as given in the description, the salts thereof, and the stereoisomers of the compounds and the salts thereof are effective inhibitors of the type 5 phosphodiesterase.

PYRROLOPYRIMIDINECARBOXAMIDES

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Page/Page column 194, (2009/10/21)

The compounds of Formula (I) wherein R1, R21, R22, R23, R24, Y and R3 have the meanings as given in the description, the salts thereof, the N-oxides of the compounds and the salts thereof and the stereoisomers of the compounds, the salts, the N-oxides of

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