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3,9-Diazabicyclo[3.3.1]nonan-7-one,3,9-dimethyl-,oxime(9CI) is an organic compound that serves as an intermediate in the synthesis of Indisetron (I532500), a 5-HT3 receptor antagonist used as an antiemetic agent. 3,9-Diazabicyclo[3.3.1]nonan-7-one,3,9-dimethyl-,oxime(9CI) plays a crucial role in the development of pharmaceuticals targeting digestive tract disorders.

141549-87-3

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141549-87-3 Usage

Uses

Used in Pharmaceutical Industry:
3,9-Diazabicyclo[3.3.1]nonan-7-one,3,9-dimethyl-,oxime(9CI) is used as an intermediate in the synthesis of Indisetron for the treatment of digestive tract disorders. Its role in the production of Indisetron makes it a valuable component in the development of antiemetic medications, which are essential for managing nausea and vomiting associated with various conditions and treatments.
Used in the Synthesis of 5-HT3 Receptor Antagonists:
3,9-Diazabicyclo[3.3.1]nonan-7-one,3,9-dimethyl-,oxime(9CI) is used as a key component in the synthesis of 5-HT3 receptor antagonists, such as Indisetron. These antagonists are crucial in the development of antiemetic drugs, which help alleviate nausea and vomiting caused by various factors, including chemotherapy, radiation therapy, and surgery. The compound's involvement in the synthesis process highlights its importance in the pharmaceutical industry for creating effective treatments for digestive tract disorders and related symptoms.

Check Digit Verification of cas no

The CAS Registry Mumber 141549-87-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,5,4 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 141549-87:
(8*1)+(7*4)+(6*1)+(5*5)+(4*4)+(3*9)+(2*8)+(1*7)=133
133 % 10 = 3
So 141549-87-3 is a valid CAS Registry Number.

141549-87-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(3,9-dimethyl-3,9-diazabicyclo[3.3.1]nonan-7-ylidene)hydroxylamine

1.2 Other means of identification

Product number -
Other names 3,9-dimethyl-3,9-diazabicyclo<3.3.1>nonan-7-one oxime

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:141549-87-3 SDS

141549-87-3Relevant academic research and scientific papers

Synthesis of (endo) 3,9-Disubstituted Diazabicyclononan-7-amines

Gregory, J. A.,Jennings, A. J.,Joiner, G. F.,King, F. D.,Rahman, S. K.

, p. 155 - 158 (1995)

The novel synthesis of a series of 3,9-diazabicyclononan-7-amines (4) is reported via an alane reduction of a key intermediate oxime (8).The stereoselectivity of the reduction is highly dependent on the size of the 3-aza substituent.

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