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391900-69-9

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391900-69-9 Usage

General Description

6-TERT-BUTYL-3-FORMYLPYRIDINE is a chemical compound with the molecular formula C12H15NO. It belongs to the group of pyridine derivatives and contains a tert-butyl group and a formyl group attached to the pyridine ring. This chemical is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is also used in the production of flavors and fragrances, and as a catalyst in various organic reactions. 6-TERT-BUTYL-3-FORMYLPYRIDINE is known for its strong and fruity odor, making it a valuable ingredient in perfumes and personal care products. It is important to handle this chemical with caution, as it may pose hazards to human health and the environment if not properly controlled.

Check Digit Verification of cas no

The CAS Registry Mumber 391900-69-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,1,9,0 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 391900-69:
(8*3)+(7*9)+(6*1)+(5*9)+(4*0)+(3*0)+(2*6)+(1*9)=159
159 % 10 = 9
So 391900-69-9 is a valid CAS Registry Number.

391900-69-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-tert-butylpyridine-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 6-TERT-BUTYLNICOTINALDEHYDE

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:391900-69-9 SDS

391900-69-9Relevant articles and documents

Lewis basicity modulation of N-heterocycles: A key for successful cross-metathesis

Lafaye, Kevin,Nicolas, Lionel,Gurinot, Amandine,Reymond, Sbastien,Cossy, Janine

supporting information, p. 4972 - 4975 (2015/01/08)

Cross-metathesis involving N-heteroaromatic olefinic derivatives is disclosed. The introduction of an appropriate substituent on the heteroaromatic ring decreases the Lewis basicity of the nitrogen atom, thus preventing the deactivation of the ruthenium-centered catalyst. The reaction is quite general in terms of both N-heterocycles and olefinic partners.

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