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Lennoxamine is a pharmaceutical chemical compound that belongs to the class of antihistamines. It is primarily used for the treatment of allergic conditions such as rhinitis and urticaria. Lennoxamine works by blocking histamine receptors in the body, which helps in reducing the symptoms of allergic reactions including sneezing, itching, and hives. Additionally, Lennoxamine is recognized for its sedative properties, making it beneficial in alleviating symptoms of insomnia and anxiety. It is generally well-tolerated by most individuals, with potential side effects being drowsiness, dry mouth, and headache. Lennoxamine is commonly available in oral tablet or liquid form and should be taken as directed by a healthcare professional.

95530-38-4

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95530-38-4 Usage

Uses

Used in Pharmaceutical Industry:
Lennoxamine is used as an antihistamine for the treatment of allergic rhinitis and urticaria, functioning by blocking histamine receptors to reduce allergic symptoms.
Lennoxamine is used as a sedative to alleviate symptoms of insomnia and anxiety due to its calming effects.
Used in Allergy Management:
Lennoxamine is used as a medication to manage allergic reactions, providing relief from sneezing, itching, and hives by inhibiting histamine action.
Used in Sleep Aid:
Lennoxamine is used as a sleep aid to help individuals suffering from insomnia, leveraging its sedative properties to promote restful sleep.
Used in Anxiety Relief:
Lennoxamine is used in the management of anxiety symptoms, offering a calming effect to those experiencing stress or anxiety.

Check Digit Verification of cas no

The CAS Registry Mumber 95530-38-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,5,3 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 95530-38:
(7*9)+(6*5)+(5*5)+(4*3)+(3*0)+(2*3)+(1*8)=144
144 % 10 = 4
So 95530-38-4 is a valid CAS Registry Number.

95530-38-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Lennoxamine

1.2 Other means of identification

Product number -
Other names (+/-)-lennoxamine

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:95530-38-4 SDS

95530-38-4Downstream Products

95530-38-4Relevant academic research and scientific papers

Synthesis of isoindolobenzazepine alkaloids based on radical reactions or Pd(0)-catalyzed reactions

Onozaki, Yu,Kurono, Nobuhito,Senboku, Hisanori,Tokuda, Masao,Orito, Kazuhiko

experimental part, p. 5486 - 5495 (2009/12/06)

(Chemical Equation Presented) Methods for synthesis of a ring system characteristic of isoindolobenzazepine alkaloids were studied. Synthesis of lennoxamine and a formal synthesis of chelenine were accomplished in a short route via radical or Pd(0)-cataly

An efficient method for the synthesis of enol ethers and enecarbamates. Total syntheses of isoindolobenzazepine alkaloids, lennoxamine and chilenine

Fuwa, Haruhiko,Sasaki, Makoto

, p. 1849 - 1853 (2008/02/10)

An efficient method for the synthesis of enol ethers and enecarbamates has been developed based on catalytic hydrosilane reduction of α-phosphonoxy enol ethers and α-phosphonoxy enecarbamates. This method has been applied to the total syntheses of two iso

A short synthesis of lennoxamine using a radical cascade

Taniguchi, Tsuyoshi,Iwasaki, Keiko,Uchiyama, Masahiko,Tamura, Osamu,Ishibashi, Hiroyuki

, p. 4389 - 4390 (2007/10/03)

(Chemical Equation Presented) A short synthesis of lennoxamine has been achieved by using a radical cascade involving aryl radical-induced 7-endo cyclization and homolytic aromatic substitution.

Total synthesis of (±)-lennoxamine and (±)-aphanorphine by intramolecular electrophilic aromatic substitution reactions of 2-amidoacroleins

Fuchs, James R.,Funk, Raymond L.

, p. 3923 - 3925 (2007/10/03)

equation presented Intramolecular electrophilic aromatic substitution reactions of 2-amidoacroleins constitute the key steps in the total syntheses of lennoxamine and aphanorphine. The aldehyde moiety of one cyclization product was transformed to a double

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