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14447-04-2

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14447-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14447-04-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,4,4 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 14447-04:
(7*1)+(6*4)+(5*4)+(4*4)+(3*7)+(2*0)+(1*4)=92
92 % 10 = 2
So 14447-04-2 is a valid CAS Registry Number.

14447-04-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name dibutyl but-2-ynedioate

1.2 Other means of identification

Product number -
Other names butynedioic acid dibutyl ester

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:14447-04-2 SDS

14447-04-2Relevant articles and documents

Total Synthesis of (+)-Trachyspic Acid 19-n-Butyl Ester

Rafaniello, Alex A.,Rizzacasa, Mark A.

, (2020)

The first total synthesis of the alkyl citrate trachyspic acid 19-n-butyl ester (1) is described. A formal [2 + 2]-cycloaddition of the silylketene acetal derived from lactone 6 with di-n-butylacetylene dicarboxylate 7 provided the cyclobutene diester 5 w

Three-Component Coupling Reactions of Aryne, DMSO, and Activated Alkyne: Stereoselective Synthesis of 2-[(o-Methylthio)aryloxy]-Substituted Dialkyl Maleates

Hazarika, Hemanta,Neog, Kashmiri,Sharma, Abhilash,Das, Babulal,Gogoi, Pranjal

, p. 5846 - 5854 (2019/05/06)

A transition-metal-free coupling reaction of aryne, DMSO, and activated alkyne for the synthesis of 2-[(o-methylthio)aryloxy]-substituted dialkyl maleates is reported. This cascade process is associated with several bond cleavage as well as bond formation

Preparation of unsymmetrical dialkyl acetylenedicarboxylates and related esters by enzymatic transesterification

Sultan, Nisrine,Thomas, Coralie,Blanco, Luis,Deloisy, Sandrine

scheme or table, p. 3443 - 3446 (2011/06/27)

An unexpected highly selective mono-transesterification of symmetrical acetylenedicarboxylates with various alcohols occurred in the presence of Candida rugosa lipase. This reaction allows an efficient preparation of unsymmetrical acetylenedicarboxylates and related α,β-acetylenic esters.

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