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Benzenamine, N-butyl-4-chloro-2-nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61511-71-5

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61511-71-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61511-71-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,5,1 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 61511-71:
(7*6)+(6*1)+(5*5)+(4*1)+(3*1)+(2*7)+(1*1)=95
95 % 10 = 5
So 61511-71-5 is a valid CAS Registry Number.

61511-71-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-butyl-4-chloro-2-nitroaniline

1.2 Other means of identification

Product number -
Other names N-Butyl-2-nitro-4-chlor-anilin

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:61511-71-5 SDS

61511-71-5Downstream Products

61511-71-5Relevant academic research and scientific papers

Synthesis and potent antifungal activity against Candida species of some novel 1H-benzimidazoles

Goeker, Hakan,Alp, Mehmet,Ates-Alagoez, Zeynep,Yildiz, Sulhiye

experimental part, p. 936 - 948 (2009/12/05)

(Chemical Equation Presented) A series of 47 novel N1-alkylated- 2-aryl-5(6)-substituted-1H-benzimidazoles and their three novel indole analogues were synthesized and evaluated for in vitro antifungal activities against Candida species by the tube dilution method. The results showed that compounds 79 and 80, having pyridine at the position C-2, of benzimidazoles exhibited the greatest activity with MIC values of 6.25-3.12 μg/mL. Indole analogues 108-110 have no inhibitory activity.

Design and syntheses of a series of novel serotonin3 antagonists

Hori,Suzuki,Yamamoto,Nakajima,Ozaki,Ohtaka

, p. 1832 - 1841 (2007/10/02)

From a structural comparison study between serotonin and serotonin3 (5- HT3) antagonists using a two-dimensional grid template composed of regular hexagons, we deduced structural modification patterns from agonists to antagonists, an

Oxidation of Aryldialkylamines with Cerium(IV) Ammonium Nitrate and Thallium(III) Nitrate

Galliani, Guido,Rindone, Bruno

, p. 828 - 832 (2007/10/02)

Nine alkylmethylanilines were oxidised with cerium(IV)ammonium nitrate and thallium(III) nitrate in acetic acid, acetonitrile, and methanol.Reaction products were those deriving from demethylation, dealkylation, and aromatic nitration at positions ortho and para to the amino-group.The ratio between demethylation and dealkylation and between them and aromatic nitration is discussed in terms of (i) the oxidising power and electrophilicity of the reagent and (ii) the co-ordinative properties of the solvent.

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