2-Chloro-4'-nitroacetanilide

Modify Date: 2025-08-22 12:59:55

2-Chloro-4'-nitroacetanilide Structure
2-Chloro-4'-nitroacetanilide structure
Common Name 2-Chloro-4'-nitroacetanilide
CAS Number 17329-87-2 Molecular Weight 214.60600
Density 1.472 g/cm3 Boiling Point 439.4ºC at 760 mmHg
Molecular Formula C8H7ClN2O3 Melting Point 185 - 186ºC
MSDS N/A Flash Point 219.6ºC

 Names

Name 2-chloro-N-(4-nitrophenyl)acetamide
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.472 g/cm3
Boiling Point 439.4ºC at 760 mmHg
Melting Point 185 - 186ºC
Molecular Formula C8H7ClN2O3
Molecular Weight 214.60600
Flash Point 219.6ºC
Exact Mass 214.01500
PSA 74.92000
LogP 2.36830
Vapour Pressure 6.39E-08mmHg at 25°C
Index of Refraction 1.63
InChIKey AZURFBCEYQYATI-UHFFFAOYSA-N
SMILES O=C(CCl)Nc1ccc([N+](=O)[O-])cc1

 Safety Information

Hazard Codes Xi: Irritant;
HS Code 2924299090

 Synthetic Route

~94%

2-Chloro-4'-nitroacetanilide Structure

2-Chloro-4'-nit...

CAS#:17329-87-2

Literature: Jin, Yi; Zhou, Zu-Yu; Tian, Wei; Yu, Qiang; Long, Ya-Qiu Bioorganic and Medicinal Chemistry Letters, 2006 , vol. 16, # 22 p. 5864 - 5869

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2-Chloro-4'-nitroacetanilide Structure

2-Chloro-4'-nit...

CAS#:17329-87-2

Literature: US5807885 A1, ; US 5807885 A

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2-Chloro-4'-nitroacetanilide Structure

2-Chloro-4'-nit...

CAS#:17329-87-2

Literature: Chemische Berichte, , vol. 48, p. 1006

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2-Chloro-4'-nitroacetanilide Structure

2-Chloro-4'-nit...

CAS#:17329-87-2

Literature: Journal of the American Chemical Society, , vol. 45, p. 1997

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2-Chloro-4'-nitroacetanilide Structure

2-Chloro-4'-nit...

CAS#:17329-87-2

Literature: Tetrahedron Letters, , vol. 39, # 32 p. 5861 - 5864

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2-Chloro-4'-nitroacetanilide Structure

2-Chloro-4'-nit...

CAS#:17329-87-2

Literature: Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), , # 4 p. 339 - 344

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2-Chloro-4'-nitroacetanilide Structure

2-Chloro-4'-nit...

CAS#:17329-87-2

Literature: Journal fuer Praktische Chemie (Leipzig), , vol. <2>137, p. 161,175

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Detail
Literature: Chemische Berichte, , vol. 48, p. 1006

 Customs

HS Code 2924299090
Summary 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 2-Chloro-4'-nitroacetanilideBioassay

View more

Name: GSH reactivity of the compound assessed as adducts formation by RP-HPLC analysis
Source: ChEMBL
Target: N/A
External Id: CHEMBL3367322
Name: Cell-based high throughput primary assay to identify activators of GPR151
Source: The Scripps Research Institute Molecular Screening Center
Target: RecName: Full=G-protein coupled receptor 151; AltName: Full=G-protein coupled receptor PGR7; AltName: Full=GPCR-2037; AltName: Full=Galanin receptor 4; AltName: Full=Galanin-receptor-like protein; Short=GalRL
External Id: GPR151_PHUNTER_AG_LUMI_1536_1X%ACT
Name: Inhibition of Dengue virus serotype 2 NS2B-NS3 protease at 50 uM
Source: ChEMBL
Target: Genome polyprotein
External Id: CHEMBL3371259
Name: Inhibition of Bovine thrombin using Boc-Val-Pro-Arg-AMC as substrate compound preincu...
Source: ChEMBL
Target: Prothrombin
External Id: CHEMBL3371261
Name: Inhibition of West Nile virus NS2B-NS3 protease at 50 uM
Source: ChEMBL
Target: Genome polyprotein
External Id: CHEMBL3371260
Name: Inhibition of human MetAP at 25 uM after 20 mins by HPLC analysis
Source: ChEMBL
Target: Methionine aminopeptidase 1
External Id: CHEMBL3367315
Name: Inhibition of Escherichia coli MetAP at 25 uM after 20 mins by HPLC analysis
Source: ChEMBL
Target: N/A
External Id: CHEMBL3367314
Name: Inhibition of wild-type Escherichia coli MurB compound preincubated for 10 mins befor...
Source: ChEMBL
Target: N/A
External Id: CHEMBL3367317
Name: Inhibition of wild-type Escherichia coli MurA compound preincubated for 10 mins befor...
Source: ChEMBL
Target: N/A
External Id: CHEMBL3367316
Name: Inhibition of wild-type Escherichia coli MurD compound preincubated for 10 mins befor...
Source: ChEMBL
Target: N/A
External Id: CHEMBL3367319
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 Synonyms

N-(4-nitrophenyl)-2-chloroacetamide
Acetanilide,2-chloro-4'-nitro
N1-(4-Nitrophenyl)-2-chloroacetamide
3-chloro-N-(3-nitrophenyl)propanamide
p-nitro-N-chloroacetylaniline
Acetamide,2-chloro-N-(4-nitrophenyl)
2-Chloro-4'-nitroacetanilide
2-Chloro-N-(4-nitrophenyl)-acetamide
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