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77-37-2

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77-37-2 Usage

Uses

Antiparkinsonian; relaxant (skeletal muscle).

Definition

ChEBI: A tertiary alcohol that consists of propan-1-ol substituted by a cyclohexyl and a phenyl group at position 1 and a pyrrolidin-1-yl group at position 3.

Synthesis

Procyclidine, 1-cyclohexyl-1-phenyl-3-pirrolidinopropan-1-ol (10.2.3), is synthesized in the exact same manner, except beginning with 2-(1-pyrrolidino) propiophenone [28–32].

Check Digit Verification of cas no

The CAS Registry Mumber 77-37-2 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 7 and 7 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 77-37:
(4*7)+(3*7)+(2*3)+(1*7)=62
62 % 10 = 2
So 77-37-2 is a valid CAS Registry Number.
InChI:InChI=1/C19H29NO/c21-19(17-9-3-1-4-10-17,18-11-5-2-6-12-18)13-16-20-14-7-8-15-20/h1,3-4,9-10,18,21H,2,5-8,11-16H2

77-37-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name procyclidine

1.2 Other means of identification

Product number -
Other names Kemadrine

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:77-37-2 SDS

77-37-2Synthetic route

1-phenyl-3-(pyrrolidin-1-yl)propan-1-one
94-39-3

1-phenyl-3-(pyrrolidin-1-yl)propan-1-one

cyclohexylmagnesium bromide
931-50-0

cyclohexylmagnesium bromide

procyclidine
77-37-2

procyclidine

Pyrrinol
6072-22-6

Pyrrinol

procyclidine
77-37-2

procyclidine

Conditions
ConditionsYield
With acetic acid; platinum Hydrogenation;
With acetic acid; platinum Hydrogenation;
ethyl 3-tetrahydro-1H-1-pyrrolilpropanoate
6317-35-7

ethyl 3-tetrahydro-1H-1-pyrrolilpropanoate

procyclidine
77-37-2

procyclidine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: diethyl ether
2: platinum; aqueous acetic acid / Hydrogenation
View Scheme
phenylmagnesium bromide

phenylmagnesium bromide

procyclidine
77-37-2

procyclidine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: diethyl ether
2: platinum; aqueous acetic acid / Hydrogenation
View Scheme
3,4,5-Trimethoxybenzoyl chloride
4521-61-3

3,4,5-Trimethoxybenzoyl chloride

procyclidine
77-37-2

procyclidine

3,4,5-trimethoxy-benzoic acid-(1-cyclohexyl-1-phenyl-3-pyrrolidino-propyl ester)

3,4,5-trimethoxy-benzoic acid-(1-cyclohexyl-1-phenyl-3-pyrrolidino-propyl ester)

Conditions
ConditionsYield
With benzene
ethyl iodide
75-03-6

ethyl iodide

procyclidine
77-37-2

procyclidine

(+/-)-1-ethyl-1-(3-cyclohexyl-3-hydroxy-3-phenyl-propyl)-pyrrolidinium; iodide
32381-63-8, 32476-62-3, 112841-59-5

(+/-)-1-ethyl-1-(3-cyclohexyl-3-hydroxy-3-phenyl-propyl)-pyrrolidinium; iodide

Conditions
ConditionsYield
With ethanol
procyclidine
77-37-2

procyclidine

methyl iodide
74-88-4

methyl iodide

(+/-)-1-(3-cyclohexyl-3-hydroxy-3-phenyl-propyl)-1-methyl-pyrrolidinium; iodide
6856-40-2

(+/-)-1-(3-cyclohexyl-3-hydroxy-3-phenyl-propyl)-1-methyl-pyrrolidinium; iodide

Conditions
ConditionsYield
With acetone
procyclidine
77-37-2

procyclidine

(S)-Procyclidine
102043-66-3

(S)-Procyclidine

procyclidine
77-37-2

procyclidine

(R)-Procyclidine
102727-66-2

(R)-Procyclidine

procyclidine
77-37-2

procyclidine

(S)-Tricylamol iodide
32381-62-7

(S)-Tricylamol iodide

Conditions
ConditionsYield
Multi-step reaction with 2 steps
2: acetone / 3 h / Ambient temperature
View Scheme
procyclidine
77-37-2

procyclidine

(R)-Tricylamol iodide
32381-60-5

(R)-Tricylamol iodide

Conditions
ConditionsYield
Multi-step reaction with 2 steps
2: 80 percent / acetone / 3 h / Ambient temperature
View Scheme

77-37-2Relevant articles and documents

Aryl-cycloalkyl-alkanolamines for treatment of cholinergic neurotoxins

-

, (2008/06/13)

A compound and method are disclosed for reducing neurotoxic effects (such as seizures and brain damage) caused by cholinergic agents such as soman (a nerve gas) and pilocarpine (a convulsant drug used to study the mechanisms of epilepsy). Effective treatment can be provided by administering an aryl-cycloalkylalkanolamine substance having the general formula: STR1 The compoudns procyclidine, biperiden, and trihexyphenidyl fall within this class of compounds. Although not previously recognized to be effective against soman or other cholinergic neurotoxins, all three representative compounds have been discovered to be highly effective against all cholinergic neurotoxins tested to data, even when administered after actual seizures begin.

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