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35567-32-9

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35567-32-9 Usage

Uses

2-(Dimethylamino)pyridine-3-carbaldehyde

Check Digit Verification of cas no

The CAS Registry Mumber 35567-32-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,5,6 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 35567-32:
(7*3)+(6*5)+(5*5)+(4*6)+(3*7)+(2*3)+(1*2)=129
129 % 10 = 9
So 35567-32-9 is a valid CAS Registry Number.

35567-32-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(dimethylamino)pyridine-3-carbaldehyde

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:35567-32-9 SDS

35567-32-9Downstream Products

35567-32-9Relevant articles and documents

Substituted Pyrrolidines and Methods of Use

-

Paragraph 2072, (2018/04/20)

The invention discloses compounds of Formula (I) wherein R1, R2, R2A, R3, R3A, R4, R4A, and R5 are as defined herein. The present invention relates to compounds and their use in the treatment of cystic fibrosis, methods for their production, pharmaceutical compositions comprising the same, and methods of treating cystic fibrosis by administering a compound of the invention.

Expedient synthesis of tetrahydroquinoline-3-spirohydantoin derivatives: Via the Lewis acid-catalyzed tert -amino effect reaction

Briones, John F.,Basarab, Gregory S.

supporting information, p. 8541 - 8544 (2016/07/13)

Magnesium triflate was found to effectively catalyze the tert-amino effect reaction (T-reaction) involving ethyl 3-(2-(dialkylamino)-phenyl)-2-nitroacrylates leading to tetrahydroquinoline nitroester derivatives. These compounds can be readily transformed

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