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[carboxyl-14C]-methyl benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18615-08-2

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18615-08-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18615-08-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,6,1 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18615-08:
(7*1)+(6*8)+(5*6)+(4*1)+(3*5)+(2*0)+(1*8)=112
112 % 10 = 2
So 18615-08-2 is a valid CAS Registry Number.

18615-08-2SDS

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 [carboxyl-14C]-benzoic acid methyl ester

1.2 Other means of identification

Product number -
Other names methyl [14C]benzoate

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:18615-08-2 SDS

18615-08-2Relevant academic research and scientific papers

A convenient method for [14C]Carbonylation reactions

Elmore, Charles S.,Dean, Dennis C.,Melillo, David G.

, p. 1135 - 1144 (2007/10/03)

A simple, efficient method for generation of 14CO from Ba14CO3 has been developed. Reduction of 14CO2 using LiBEt3H gave [14C]formate in good yield which was treated with conc. H2SO4 to effect dehydration to 14CO. Through direct attachment of a reaction vessel containing aryl substrate and Pd(0) catalyst, [14C]carbonylation reactions were performed without the use of a mercury transfer pump. [14C]Carbonylation reactions using 14CO generated in this manner have been shown to proceed in good yield with a variety of substrates.

Syntheses of N-t-butyl-α-phenylnitrone-α-14C and α-(4-pyridyl-1-oxide)-N-t-butylnitrone-α-14C

Le, Diem Duy,Zhang, Yinsheng,Chien, David H.,Moravek, Josef

, p. 1119 - 1125 (2007/10/03)

N-t-Butyl-α-phenylnitrone-α-14C was prepared from benzoic-α-14C acid via benzyl alcohol in 40 - 55% yield (sp. activity: 30 mCi/mmol). α-(4-Pyridyl-1-oxide)-N-t-butylnitrone-α-14C arrived from Ba14CO3

Synthesis of optically pure (D-phenyl[3-14C]alanine

Koltai,Alexin,Rutkai,Toth-Sarudy

, p. 977 - 982 (2007/10/03)

Lithium aluminium hydride reduction of methyl [7-14C]benzoate gave [7-14C]benzyl alcohol which was transformed (HBr, H2SO4) to [7-14C]benzyl bromide. The latter was reacted with lithium N-(bis-methylt

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