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Carbonic acid benzylhexyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67987-31-9

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67987-31-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67987-31-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,9,8 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 67987-31:
(7*6)+(6*7)+(5*9)+(4*8)+(3*7)+(2*3)+(1*1)=189
189 % 10 = 9
So 67987-31-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H20O3/c1-2-3-4-8-11-16-14(15)17-12-13-9-6-5-7-10-13/h5-7,9-10H,2-4,8,11-12H2,1H3

67987-31-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl hexyl carbonate

1.2 Other means of identification

Product number -
Other names Kohlensaeure-benzyl-hexylester

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:67987-31-9 SDS

67987-31-9Downstream Products

67987-31-9Relevant academic research and scientific papers

Photo-on-Demand Synthesis of Chloroformates with a Chloroform Solution Containing an Alcohol and Its One-Pot Conversion to Carbonates and Carbamates

Liang, Fengying,Suzuki, Yuto,Tsuda, Akihiko,Yanai, Masaki

supporting information, (2020/04/21)

Chloroformates are key reagents for synthesizing carbonates and carbamates. The present study reports a novel photo-on-demand in situ synthesis of chloroformates with a CHCl3 solution containing a primary alkyl alcohol. It further allowed the one-pot synthesis of carbonates and carbamates through subsequent addition of alcohols or amines, respectively.

Mild and efficient capture and functionalisation of CO2 using silver(i) oxide and application to 13C-labelled dialkyl carbonates

Tunbridge, Gemma A.,Baruchello, Riccardo,Caggiano, Lorenzo

, p. 4613 - 4621 (2013/05/08)

A high yielding three-component reaction between β-iodo ethylamine derivatives, MeOH and gaseous CO2 at ambient temperatures and pressures is reported using silver(i) oxide. Unfunctionalised alkyl iodides were also found to be effective in this transformation and their optimisation is also described. To highlight the ease and control with which gaseous CO 2 can be captured and functionalised under mild conditions, the reaction was performed using 13C-enriched CO2 to afford specifically 13C-carbonyl-labelled dialkyl carbonates with exquisite control of the isotopic purity in good yields and without the need for specialised equipment.

Applications of Phase Transfer Catalysis. 15. Phase Transfer Catalytic Preparation of Carbonic Esters Without the Use of Phosgene

Lissel, Manfred,Dehmlow, Eckehard V.

, p. 1210 - 1215 (2007/10/02)

Carbonic esters can be prepared in a phase-transfer catalytic reaction from primary alkyl halides and a mixture of dry potassium hydrogen carbonate and dry potassium carbonate in non-polar solvents.The conversion is ineffective in the absence of hydrogen carbonate and catalyst.

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