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212914-74-4

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212914-74-4 Usage

Uses

4-(Hydroxymethyl)-2-pyridinecarboxaldehyde is a reactant that has been used in the preparation of edotecarin analogues as potent topoisomerase I inhibitors with cytotoxic (CTX) activities against MKN-45 human stomach cancer or MX-1 human breast cancer.

Check Digit Verification of cas no

The CAS Registry Mumber 212914-74-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,2,9,1 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 212914-74:
(8*2)+(7*1)+(6*2)+(5*9)+(4*1)+(3*4)+(2*7)+(1*4)=114
114 % 10 = 4
So 212914-74-4 is a valid CAS Registry Number.

212914-74-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(hydroxymethyl)pyridine-2-carbaldehyde

1.2 Other means of identification

Product number -
Other names 4-hydroxymethylpyridine-2-carbaldehyde

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:212914-74-4 SDS

212914-74-4Downstream Products

212914-74-4Relevant articles and documents

Selective DIBAL-H Monoreduction of a Diester Using Continuous Flow Chemistry: From Benchtop to Kilo Lab

Uhlig, Nick,Martins, Andrew,Gao, Detian

, p. 2326 - 2335 (2020/06/08)

Herein we report a selective DIBAL-H-mediated reduction of a heterocyclic diester to the corresponding monoaldehyde using continuous flow chemistry. The use of continuous flow enabled operation at lower temperatures and better control of the reaction time, thereby allowing for a significant increase in reaction selectivity and yield compared with batch conditions. The reaction's development as a continuous flow process and its scale-up from laboratory gram scale to multikilogram scale are discussed, including design of experiments studies to probe the optimal reaction window.

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