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844500-75-0

Methyl (4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbaMate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • Methyl (4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate

    Cas No: 844500-75-0

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  • methyl (4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate

    Cas No: 844500-75-0

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  • 844500-75-0 Structure

  • Basic information

    1. Product Name: Methyl (4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbaMate
    2. Synonyms: Methyl (4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbaMate
    3. CAS NO:844500-75-0
    4. Molecular Formula: C14H20BNO4
    5. Molecular Weight: 277.1239
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 844500-75-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 345.2±25.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.11±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 14.00±0.70(Predicted)
    10. CAS DataBase Reference: Methyl (4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbaMate(CAS DataBase Reference)
    11. NIST Chemistry Reference: Methyl (4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbaMate(844500-75-0)
    12. EPA Substance Registry System: Methyl (4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbaMate(844500-75-0)

  • 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: 844500-75-0(Hazardous Substances Data)

844500-75-0 Usage

General Description

Methyl (4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbaMate is a chemical compound used in organic synthesis and pharmaceutical research. It is a methyl carbamate derivative containing a boronate ester functionality. Methyl (4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbaMate has potential applications in the development of new drugs and in the synthesis of complex organic molecules. Its unique structure and reactivity make it a valuable building block in the creation of novel chemical compounds with biological activity. Additionally, the boronate ester group in this compound can serve as a site for selective chemical transformations, making it a versatile tool in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 844500-75-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,4,5,0 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 844500-75:
(8*8)+(7*4)+(6*4)+(5*5)+(4*0)+(3*0)+(2*7)+(1*5)=160
160 % 10 = 0
So 844500-75-0 is a valid CAS Registry Number.

844500-75-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborlan-2-yl)phenylcarbamate

1.2 Other means of identification

Product number -
Other names methyl(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate

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:844500-75-0 SDS

844500-75-0Relevant articles and documents

Outer-sphere direction in iridium C-H borylation

Roosen, Philipp C.,Kallepalli, Venkata A.,Chattopadhyay, Buddhadeb,Singleton, Daniel A.,Maleczka, Robert E.,Smith, Milton R.

supporting information; experimental part, p. 11350 - 11353 (2012/08/29)

The NHBoc group affords ortho selective C-H borylations in arenes and alkenes. Experimental and computational studies support an outer sphere mechanism where the N-H proton hydrogen bonds to a boryl ligand oxygen. The regioselectivities are unique and com

Substituted Benzo-Imidazo-Pyrido-Diazepine Compounds

-

Page/Page column 135-136, (2012/05/07)

The present invention relates to substituted benzo-imidazo-pyrido-diazepine compounds and methods of synthesizing these compounds. The present invention also relates to pharmaceutical compositions containing substituted benzo-imidazo-pyrido-diazepine compounds and methods of treating cell proliferative disorders, such as cancer, by administering these compounds and pharmaceutical compositions to subjects in need thereof.

PYRAZOLOPYRIMIDINE ANALOGS AND THEIR USE AS MTOR KINASE AND PI3 KINASE INHIBITORS

-

Page/Page column 85-86, (2008/12/08)

The present invention relates to Pyrazolopyrimidine Analogs, methods of making Pyrazolopyrimidine Analogs, compositions comprising a Pyrazolopyrimidine Analog, and methods for treating mTOR-related disorders comprising administering to a subject in need thereof an effective amount of a Pyrazolopyrimidine Analog. The invention also relates to treating PI3K-related disorders comprising administering to a subject in need thereof an effective amount of a Pyrazolopyrimidine Analog.

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