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15561-33-8

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15561-33-8 Usage

Chemical Class

Alcohols

Primary Use

Antihistamine for allergy symptoms

Additional Use

Sedative effect

Common Symptoms Relieved

Sneezing, itching, runny nose

Mechanism of Action

Blocks histamine action

Common Combinations

Other medications for colds, hay fever, and allergies

Administration Route

Oral (tablets or syrup)

Precautions

May cause drowsiness and impair cognitive function

Check Digit Verification of cas no

The CAS Registry Mumber 15561-33-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,5,6 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 15561-33:
(7*1)+(6*5)+(5*5)+(4*6)+(3*1)+(2*3)+(1*3)=98
98 % 10 = 8
So 15561-33-8 is a valid CAS Registry Number.

15561-33-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-8-methoxy-4-methyl-5H-pyrido<4,3-b>indole

1.2 Other means of identification

Product number -
Other names chloro-1 phenyl-2 propanol-2

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:15561-33-8 SDS

15561-33-8Relevant articles and documents

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Ishida

, p. 924 (1960)

-

Efficient conversion of alkenes to chlorohydrins by a Ru-based artificial enzyme

Lopez, Sarah,Rondot, Laurianne,Cavazza, Christine,Iannello, Marina,Boeri-Erba, Elisabetta,Burzlaff, Nicolai,Strinitz, Frank,Jorge-Robin, Adeline,Marchi-Delapierre, Caroline,Ménage, Stéphane

supporting information, p. 3579 - 3582 (2017/03/31)

Artificial enzymes are required to catalyse non-natural reactions. Here, a hybrid catalyst was developed by embedding a novel Ru complex in the transport protein NikA. The protein scaffold activates the bound Ru complex to produce a catalyst with high regio- and stereo-selectivity. The hybrid efficiently and stably produced α-hydroxy-β-chloro chlorohydrins from alkenes (up to 180 TON with a TOF of 1050 h?1).

External trapping of halomethyllithium enabled by flow microreactors

Degennaro, Leonardo,Fanelli, Flavio,Giovine, Arianna,Luisi, Renzo

supporting information, p. 21 - 27 (2015/01/30)

This work demonstrates that the accurate control of the reaction parameters realized within microreactor systems allowed for a taming of the reactivity of thermally unstable intermediates such as haloalkyllithiums. The first example of effective external trapping of a reactive carbenoid such as the chloromethyllithium is described. By using microreactor systems, a continuous flow synthesis of chloro alcohols and chloro amines could be achieved with high yields. By controlling the residence time the highly reactive chloromethyllithium could be generated and reacted with electrophiles at temperatures much higher than in batch-mode and without internal quenching. The developed continuous-flow process matches the requirements for sustainability.

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