Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1036648-31-3

4-(tert-butyldimethylsilyloxy)cyclohexyl 4-methylbenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1036648-31-3 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 1036648-31-3 Structure

  • Basic information

    1. Product Name: 4-(tert-butyldimethylsilyloxy)cyclohexyl 4-methylbenzoate
    2. Synonyms: 4-(tert-butyldimethylsilyloxy)cyclohexyl 4-methylbenzoate
    3. CAS NO:1036648-31-3
    4. Molecular Formula:
    5. Molecular Weight: 348.558
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1036648-31-3.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: 4-(tert-butyldimethylsilyloxy)cyclohexyl 4-methylbenzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(tert-butyldimethylsilyloxy)cyclohexyl 4-methylbenzoate(1036648-31-3)
    11. EPA Substance Registry System: 4-(tert-butyldimethylsilyloxy)cyclohexyl 4-methylbenzoate(1036648-31-3)

  • 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: 1036648-31-3(Hazardous Substances Data)

1036648-31-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1036648-31-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,6,6,4 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1036648-31:
(9*1)+(8*0)+(7*3)+(6*6)+(5*6)+(4*4)+(3*8)+(2*3)+(1*1)=143
143 % 10 = 3
So 1036648-31-3 is a valid CAS Registry Number.

1036648-31-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(tert-butyldimethylsilyloxy)cyclohexyl 4-methylbenzoate

1.2 Other means of identification

Product number -
Other names -

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:1036648-31-3 SDS

1036648-31-3Relevant articles and documents

Organic electrosynthesis using toluates as simple and versatile radical precursors

Lam, Kevin,Marko, Istvan E.

supporting information; experimental part, p. 95 - 97 (2009/03/11)

The electrolysis of toluate esters leads smoothly to the formation of the radical of the alkyl fragment. This property has been used to develop a new electrochemical deoxygenation reaction. The Royal Society of Chemistry.

Chemoselective chemical and electrochemical deprotections of aromatic esters

Lam, Kevin,Marko, Istvan E.

supporting information; experimental part, p. 2752 - 2755 (2009/11/30)

Alcohols can be easily and chemoselectively deprotected from the corresponding aromatic esters by using either SmI2/HMPA or by electrolysis In the presence of a proton source.

Toluates: unexpectedly versatile reagents

Lam, Kevin,Markó, István E.

supporting information; experimental part, p. 10930 - 10940 (2010/02/28)

The mechanism of the monoelectronic reduction of aromatic esters has been investigated. The unexpected synthetic utility of the toluate moiety in the deoxygenation of alcohols and the allylation of ketones is also reported. Finally, the use of aromatic esters as robust, though easily removable, protecting groups is depicted.

Using toluates as simple and versatile radical precursors

Lam, Kevin,Marko, Istvan E.

supporting information; experimental part, p. 2773 - 2776 (2009/05/30)

(Chemical Equation Presented) The viability of the toluate moiety as a radical precursor has been examined by studying deoxygenation and cyclization reactions.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 1036648-31-3