14338-32-0,MFCD00011984
Catalog No.:AA007YUD

14338-32-0 | 2-Chloro-1-methylpyridinium iodide

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
98%(HPLC)
in stock  
$24.00   $17.00
- +
25g
98%
in stock  
$51.00   $36.00
- +
100g
98%
in stock  
$135.00   $95.00
- +
500g
98%
in stock  
$527.00 $369.00
  • Technical Information
  • Properties
  • Literature
  • Application
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA007YUD
Chemical Name:
2-Chloro-1-methylpyridinium iodide
CAS Number:
14338-32-0
Molecular Formula:
C6H7ClIN
Molecular Weight:
255.4839
MDL Number:
MFCD00011984
SMILES:
Clc1cccc[n+]1C.[I-]
NSC Number:
200739
Properties
Computed Properties
 
Complexity:
74.9  
Covalently-Bonded Unit Count:
2  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
0  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  

Synonyms
 
  
Literature
Application
2-Chloro-1-methylpyridinium iodide, commonly known as the Mukaiyama reagent, is a versatile compound widely employed in organic synthesis due to its ability to activate hydroxy groups in alcohols and carboxylic acids. This reagent facilitates the synthesis of various derivatives including esters, lactones, amides, lactams, and ketenes from their corresponding carboxylic acids. Additionally, it serves as an efficient coupling reagent in peptide synthesis, offering advantages such as low toxicity, straightforward reaction conditions, and cost-effectiveness compared to alternatives like EDC.

In applications beyond organic synthesis, 2-Chloro-1-methylpyridinium iodide finds utility as a dehydrating agent for converting aldoximes to nitriles and alcohols to alkyl thiocyanates. Moreover, it serves as a cross-linking agent for producing biodegradable cross-linked hyaluronic acid film and gelatin membranes, offering potential in biomedical applications. Furthermore, it acts as a condensing agent in the synthesis of various β-lactams from β-amino acids, showcasing its versatility in diverse chemical processes.
Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
SDS
Related Products of 14338-32-0
Historical Records
Tags:14338-32-0 Molecular Formula|14338-32-0 MDL|14338-32-0 SMILES|14338-32-0 2-Chloro-1-methylpyridinium iodide
Catalog No.: AA007YUD
14338-32-0,MFCD00011984
14338-32-0 | 2-Chloro-1-methylpyridinium iodide
Pack Size: 5g
Purity: 98%(HPLC)
in stock
$24.00 $17.00
Pack Size: 25g
Purity: 98%
in stock
$51.00 $36.00
Pack Size: 100g
Purity: 98%
in stock
$135.00 $95.00
Pack Size: 500g
Purity: 98%
in stock
$527.00 $369.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA007YUD
Chemical Name: 2-Chloro-1-methylpyridinium iodide
CAS Number: 14338-32-0
Molecular Formula: C6H7ClIN
Molecular Weight: 255.4839
MDL Number: MFCD00011984
SMILES: Clc1cccc[n+]1C.[I-]
NSC Number: 200739
Properties
Complexity: 74.9  
Covalently-Bonded Unit Count: 2  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 1  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 0  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
71:   
Application fold
2-Chloro-1-methylpyridinium iodide, commonly known as the Mukaiyama reagent, is a versatile compound widely employed in organic synthesis due to its ability to activate hydroxy groups in alcohols and carboxylic acids. This reagent facilitates the synthesis of various derivatives including esters, lactones, amides, lactams, and ketenes from their corresponding carboxylic acids. Additionally, it serves as an efficient coupling reagent in peptide synthesis, offering advantages such as low toxicity, straightforward reaction conditions, and cost-effectiveness compared to alternatives like EDC.

In applications beyond organic synthesis, 2-Chloro-1-methylpyridinium iodide finds utility as a dehydrating agent for converting aldoximes to nitriles and alcohols to alkyl thiocyanates. Moreover, it serves as a cross-linking agent for producing biodegradable cross-linked hyaluronic acid film and gelatin membranes, offering potential in biomedical applications. Furthermore, it acts as a condensing agent in the synthesis of various β-lactams from β-amino acids, showcasing its versatility in diverse chemical processes.
Building Blocks More >
135481-57-1
135481-57-1
6-Benzyl-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine-2,4(1h,3h)-dione
AA007ZI5 | MFCD06657750
134135-41-4
134135-41-4
5-(Bromomethyl)thiophene-2-carbonitrile
AA008003 | MFCD08236857
133405-86-4
133405-86-4
1H-1,5-Benzodiazepine, 2,3,4,5-tetrahydro-3-methyl-
AA0080GB | MFCD20441501
120589-86-8
120589-86-8
4-Acetyl-3,4-dihydroquinoxalin-2(1H)-one
AA0080V1 | MFCD01995115
120315-65-3
120315-65-3
4-Bromo-3-methoxybenzonitrile
AA00812Z | MFCD09753723
1125-28-6
1125-28-6
1-(1,3,5-Trimethyl-1h-pyrazol-4-yl)ethanone
AA0082AJ | MFCD00462201
106848-38-8
106848-38-8
1-benzyl-4-bromoimidazole
AA0082X4 | MFCD09033094
1083197-78-7
1083197-78-7
4-Trifluoromethyl-3-formylpyridine
AA0083M7 | MFCD07781251
1060815-08-8
1060815-08-8
2-Bromo-6-fluoroimidazo[1,2-a]pyridine
AA0084BX | MFCD10698610
10590-69-9
10590-69-9
4-Methylquinoline-2-carbonitrile
AA0084V8 | MFCD08705686
Submit
© 2017 AA BLOCKS, INC. All rights reserved.