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2,6-bis(tert-butylamino)-4-methylpyridin-3-yl methyl ketone, also known as BBS, is a chemical compound that is widely utilized in the pharmaceutical industry. It serves as a fundamental building block for the synthesis of a variety of drugs and active pharmaceutical ingredients. This yellowish solid is soluble in organic solvents and is characterized by its molecular formula, C16H26N2O. BBS is particularly valued for its capacity to function as a ligand in metal-catalyzed reactions and for its contribution to the creation of a broad range of chemical structures. Its distinctive structure and properties render it a highly versatile and valuable chemical in the realms of organic synthesis and drug development. Furthermore, BBS is employed in the synthesis of intermediate products for the production of agrochemicals, fragrances, and dyes.

58253-99-9

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58253-99-9 Usage

Uses

Used in Pharmaceutical Industry:
2,6-bis(tert-butylamino)-4-methylpyridin-3-yl methyl ketone is used as a building block for the synthesis of various drugs and active pharmaceutical ingredients. Its role in creating diverse chemical structures makes it a valuable component in drug development.
Used in Organic Synthesis:
2,6-bis(tert-butylamino)-4-methylpyridin-3-yl methyl ketone is used as a ligand in metal-catalyzed reactions, contributing to the formation of a wide array of chemical structures. Its versatility in organic synthesis is highly appreciated.
Used in Agrochemical Production:
2,6-bis(tert-butylamino)-4-methylpyridin-3-yl methyl ketone is used as an intermediate product in the synthesis of agrochemicals, playing a crucial role in the development of effective agricultural products.
Used in Fragrance and Dye Industries:
2,6-bis(tert-butylamino)-4-methylpyridin-3-yl methyl ketone is used in the synthesis of intermediate products for the production of fragrances and dyes, enhancing the variety and quality of these products.

Check Digit Verification of cas no

The CAS Registry Mumber 58253-99-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,2,5 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 58253-99:
(7*5)+(6*8)+(5*2)+(4*5)+(3*3)+(2*9)+(1*9)=149
149 % 10 = 9
So 58253-99-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H27N3O/c1-10-9-12(18-15(3,4)5)17-14(13(10)11(2)20)19-16(6,7)8/h9H,1-8H3,(H2,17,18,19)

58253-99-9SDS

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 1-[2,6-bis(tert-butylamino)-4-methylpyridin-3-yl]ethanone

1.2 Other means of identification

Product number -
Other names 2,6-Di-tert.-butylamino-3-acetyl-4-methylpyridin

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:58253-99-9 SDS

58253-99-9Downstream Products

58253-99-9Relevant academic research and scientific papers

4-Alkyl-2,6-di(secondary or tertiary alkylamino) pyridines, compositions thereof and methods for treating diabetes and obesity

-

, (2008/06/13)

Compounds of the formula STR1 wherein R is secondary alkyl of 3 to 7 carbon atoms or tertiary alkyl of 4 to 7 carbon atoms, R' is secondary alkyl of 3 to 7 carbon atoms or tertiary alkyl of 4 to 7 carbon atoms, R1 is alkyl of 1 to 4 carbon atoms, R2 is hydrogen, chloro or bromo, and R3 is hydrogen, --CO--R4 or cyano, Wherein R4 is alkyl of 1 to 4 carbon atoms, alkoxy of 1 to 3 carbon atoms, STR2 OR AMINO, WHEREIN EACH X is independently alkyl of 1 to 3 carbon atoms, alkoxy of 1 to 3 carbon atoms or halo or two X's on adjacent carbon atoms together are methylenedioxy, with the proviso that the ortho positions of the phenyl ring are free of halo substituents, and n is 0, 1, 2 or 3, And the pharmaceutically acceptable acid addition salts thereof, Are useful as anti-obesity and anti-diabetic agents. The compounds wherein R2 is hydrogen and R3 is alkylcarbonyl, benzoyl or substituted benzoyl are synthesized from ketoketenimines and amidines while those wherein R2 is hydrogen and R3 is alkylcarbonyl are also synthesized from isoxazolium salts and ammonia. The compounds wherein R2 is hydrogen and R3 is cyano are synthesized from the corresponding 2,6-dihalopyridines as are many of the other compounds. The compounds wherein R2 is hydrogen and R3 is alkylcarbonyl, alkoxycarbonyl or carbamoyl are synthesized from the corresponding cyano compounds. The compounds wherein R2 is hydrogen and R3 is (C2-4 alkyl) carbonyl are also synthesized from the corresponding compounds wherein R3 is acetyl. The compounds wherein R2 is chloro or bromo are synthesized from the corresponding compounds wherein R2 is hydrogen and an N-halosuccinimide. The compounds wherein R3 is hydrogen are synthesized from the corresponding alkylcarbonyl compounds or 2,6-dihalopyridines.

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