CHLOROACETALDEHYDE OXIME

Base Information

• Chemical Name: CHLOROACETALDEHYDE OXIME
• CAS No.: 51451-05-9
• Molecular Formula: C2H4ClNO
• Molecular Weight: 93.5129
• Hs Code.: 2928000090
• Mol file: 51451-05-9.mol

Synonyms:CHLOROACETALDEHYDE OXIME

Chemical Property of CHLOROACETALDEHYDE OXIME

Chemical Property:

• PSA: 32.59000
• LogP: 0.68520

Purity/Quality:

98%Min ^*data from raw suppliers

CHLOROACETALDEHYDE OXIME 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of CHLOROACETALDEHYDE OXIME

There total 5 articles about CHLOROACETALDEHYDE OXIME which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 84.0%

Acetaldehyde oxime (107-29-9) → chloroacetaldoxime (51451-05-9)

Guidance literature:

With hydrogenchloride; potassium permanganate; sodium hydroxide; In water; at -2 ℃;

Reference yield:

2-chloroethanal (107-20-0) → chloroacetaldoxime (51451-05-9)

Guidance literature:

With hydroxylamine;

Reference yield:

→ chloroacetaldoxime (51451-05-9)

Guidance literature:

With hydroxylamine hydrochloride; water;

upstream raw materials:

2-chloroethanal

water

Acetaldehyde oxime

Downstream raw materials:

formaldehyd

hydrogen cyanide

trans-nitrosoethylene

2-chloroethanal

Refernces

• 1、 -. "Chemically synthesized heterocyclic insecticide intermediate and preparation method thereof". Paragraph 0043. . Retrieved 2017/11/29.
• 2、 Lilienkampf, Annamaria,Jialin, Mao,Baojie, Wan,Yuehong, Wang,Franzblau, Scott G.,Kozikowski, Alan P.. "Structure-Activity relationships for a series of quinoline-based compounds active against replicating and nonreplicating mycobacterium tuberculosis". supporting information; experimental part. p. 2109 - 2118. Retrieved 2009/12/31.