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1116572-42-9

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1116572-42-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1116572-42-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,1,6,5,7 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1116572-42:
(9*1)+(8*1)+(7*1)+(6*6)+(5*5)+(4*7)+(3*2)+(2*4)+(1*2)=129
129 % 10 = 9
So 1116572-42-9 is a valid CAS Registry Number.

1116572-42-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methyl-2-propyl-3-pyridinecarboxylic acid ethyl ester

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:1116572-42-9 SDS

1116572-42-9Downstream Products

1116572-42-9Relevant articles and documents

Tailor-made synthesis of fully alkylated/arylated nicotinates by FeCl3-mediated condensation of enamino esters with enones

Hirai, Sho,Horikawa, Yurie,Asahara, Haruyasu,Nishiwaki, Nagatoshi

, p. 2390 - 2393 (2017)

A new method for synthesizing polyalkylated/arylated nicotinates is established using a condensation of enamino esters with enones in the presence of FeCl3. This method facilitates the introduction of alkyl or aryl groups at any position on demand, which has not been achieved by other procedures.

The preparation of 1,2,4-triazines from α,β-diketo-ester equivalents and their application in pyridine synthesis

Altuna-Urquijo, Marta,Stanforth, Stephen P.,Tarbit, Brian

, p. 6111 - 6113 (2007/10/03)

The α-Chloro-α-acetoxy-β-keto-esters were prepared from β-keto-esters in good overall yields. These compounds reacted as α,β-diketo-ester equivalents with amidrazones yielding triazines, generally in good yields, or with an amidrazone and 2,5-norbornadien

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