1032903-50-6

  • Product Name:1-Chloro-5-isopropoxy-2-methyl-4-nitrobenzene
  • Molecular Formula:C10H12ClNO3
  • Molecular Weight:229.663
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Product Details

Purity:99%

1032903-50-6 In Stock, 1-Chloro-5-isopropoxy-2-methyl-4-nitrobenzene Good Manufacturer

  • Molecular Formula:C10H12ClNO3
  • Molecular Weight:229.663
  • Boiling Point:333.1 °C at 760 mmHg 
  • Flash Point:155.3 °C 
  • PSA:55.05000 
  • Density:1.228 g/cm3 
  • LogP:3.86700 

1-Chloro-5-isopropoxy-2-methyl-4-nitrobenzene(Cas 1032903-50-6) Usage

InChI:InChI=1S/C10H12ClNO3/c1-6(2)15-10-5-8(11)7(3)4-9(10)12(13)14/h4-6H,1-3H3

1032903-50-6 Relevant articles

Novel sulfinyl anilino pyrimidine derivative and application thereof in preparation of antitumor drugs

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Paragraph 0035; 0046-0048, (2021/10/16)

The invention relates to the field of me...

CONDENSED-RING PYRIMIDYLAMINO DERIVATIVE, PREPARATION METHOD THEREFOR, AND INTERMEDIATE, PHARMACEUTICAL COMPOSITION AND APPLICATIONS THEREOF

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Paragraph 0164; 0165, (2018/03/25)

Disclosed are a condensed-ring pyrimidyl...

HYDRATE OF 2-ISOPROPOXY-5-METHYL-4-(PIPERIDIN-4-YL) ANILINE DIHYDROCHLORIDE, PREPARATION METHOD AND USE OF THE SAME

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Paragraph 0046-0049, (2018/04/20)

The present invention relates to 2-isopr...

Preparation method of 2-isopropoxy-5-methyl-4-(piperidine-4-yl) aniline dihydrochloride

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Paragraph 0026; 0027; 0028, (2017/08/29)

The invention relates to a preparation m...

1032903-50-6 Process route

isopropyl alcohol
67-63-0,8013-70-5

isopropyl alcohol

1-chloro-5-fluoro-2-methyl-4-nitrobenzene
112108-73-3

1-chloro-5-fluoro-2-methyl-4-nitrobenzene

1-chloro-2-methyl-4-nitro-5-(propan-2-yloxy)benzene
1032903-50-6

1-chloro-2-methyl-4-nitro-5-(propan-2-yloxy)benzene

Conditions
Conditions Yield
With caesium carbonate; at 60 ℃;
95%
With caesium carbonate; at 60 ℃; for 16h;
95%
With potassium hydroxide; at 20 ℃;
86.3%
With caesium carbonate; for 10h; Reflux;
83%
With caesium carbonate; at 60 ℃;
82%
With caesium carbonate; at 60 ℃;
82%
With caesium carbonate; at 60 ℃; for 24h;
74.4%
With caesium carbonate; at 60 ℃;
 
With potassium carbonate; for 40h; Reflux;
 
With potassium carbonate; for 40h; Reflux;
 
2-chloro-4-fluorotoluene
452-73-3

2-chloro-4-fluorotoluene

1-chloro-2-methyl-4-nitro-5-(propan-2-yloxy)benzene
1032903-50-6

1-chloro-2-methyl-4-nitro-5-(propan-2-yloxy)benzene

Conditions
Conditions Yield
Multi-step reaction with 2 steps
1: sulfuric acid; potassium nitrate / 0 - 20 °C
2: caesium carbonate / 60 °C
With sulfuric acid; caesium carbonate; potassium nitrate;
 
Multi-step reaction with 2 steps
1: sulfuric acid; potassium nitrate / 22 h / 0 - 20 °C
2: caesium carbonate / 24 h / 60 °C
With sulfuric acid; caesium carbonate; potassium nitrate;
 
Multi-step reaction with 2 steps
1: sulfuric acid; nitric acid / Cooling with ice
2: potassium carbonate / 40 h / Reflux
With sulfuric acid; nitric acid; potassium carbonate;
 
Multi-step reaction with 2 steps
1: sulfuric acid; nitric acid / Cooling with ice
2: potassium carbonate / 40 h / Reflux
With sulfuric acid; nitric acid; potassium carbonate;
 

1032903-50-6 Upstream products

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  • 112108-73-3
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