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3-Nitroheptan-4-ol is an organic compound with the molecular formula C7H15NO3. It is a colorless liquid at room temperature and has a molecular weight of 159.2 g/mol. 3-nitroheptan-4-ol is characterized by the presence of a nitro group (-NO2) at the third carbon position and a hydroxyl group (-OH) at the fourth carbon position in a heptane (seven-carbon) chain. 3-Nitroheptan-4-ol is synthesized through various chemical reactions and is used in the production of pharmaceuticals, explosives, and other chemical compounds. Due to its reactive nature, it is considered hazardous and requires proper handling and storage to prevent potential health and environmental risks.

5462-04-4

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5462-04-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5462-04-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5462-04:
(6*5)+(5*4)+(4*6)+(3*2)+(2*0)+(1*4)=84
84 % 10 = 4
So 5462-04-4 is a valid CAS Registry Number.

5462-04-4SDS

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 3-nitroheptan-4-ol

1.2 Other means of identification

Product number -
Other names 4-Heptanol,3-nitro

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:5462-04-4 SDS

5462-04-4Downstream Products

5462-04-4Relevant academic research and scientific papers

Dynamic kinetic asymmetric ring-opening/reductive amination sequence of racemic nitroepoxides with chiral amines: Enantioselective synthesis of chiral vicinal diamines

Agut, Juan,Vidal, Andreu,Rodríguez, Santiago,González, Florenci V.

, p. 5717 - 5722 (2013/07/25)

We report a highly diastereoselective synthesis of vicinal diamines by the treatment of nitroepoxides with primary amines and then a reducing agent. When using a chiral primary amine, racemic nitroepoxides are transformed into chiral diamines as a single enantiomers (>95:5 er) through a dynamic kinetic asymmetric transformation (DYKAT). The overall process is a one-pot procedure combining the exposure of nitroepoxides to chiral amines to afford diastereomeric mixtures of aminoimines and subsequent stereoselective imine reduction.

Facile regiocontrolled synthesis of trialkyl-substituted pyrazines

Elmaaty, Tarek Abou,Castle, Lyle W.

, p. 5529 - 5530 (2007/10/03)

(Chemical Equation Presented) α-Nitro ketones can be transformed selectively into trialkyl-substituted pyrazines via reaction with α-amino ketones using octyl viologen as an electron-transfer reagent. The new synthetic method, and the optimal reaction conditions that allow for the regiochemical control, are described.

Method of producing organic compounds in presence of oxyethylene ether catalyst and in a solvent minimized environment

-

Page 8-9, (2008/06/13)

A process of producing organic compounds, such as acetaminophen, nitroalcohols and indoles, employs a catalyst system of an oxyethylene ether and a metal containing inorganic or organic reagent. The oxyethylene ether at least partially complexes the metal of the inorganic or organic reagent. As such, the reactions may be conducted neat. The processes are environmentally friendly and operationally simple.

Use of heterogeneous catalyst KG-60-NEt2 in Michael and Henry reactions involving nitroalkanes

Ballini, Roberto,Bosica, Giovanna,Livi, Damiana,Palmieri, Alessandro,Maggi, Raimondo,Sartori, Giovanni

, p. 2271 - 2273 (2007/10/03)

The N,N-diethylpropylamine supported on amorphous silica (KG-60-NEt2) catalyses the formation of carbon-carbon bonds by nitroalkanes through both the nitroaldol (Henry) and Michael reactions. The catalyst shows general utility with a variety of electrophilic acceptors. Moreover, the catalyst can be reused for two further cycles without loss of the activity.

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