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3321-06-0

3321-06-0

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3321-06-0 Usage

General Description

Denaverine is a synthetic vasodilator and antispasmodic medication that works by relaxing and widening the blood vessels, thus improving blood flow and reducing muscle spasms. It is commonly used to treat conditions such as intermittent claudication, a condition characterized by cramping and pain in the legs during physical activity due to reduced blood flow, as well as peripheral vascular disease and Raynaud's phenomenon. Denaverine may also be used in combination with other medications to treat labor pains and complications during childbirth. It is typically administered through injection or intravenous infusion and has been shown to be well-tolerated with few reported side effects.

Check Digit Verification of cas no

The CAS Registry Mumber 3321-06-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,2 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3321-06:
(6*3)+(5*3)+(4*2)+(3*1)+(2*0)+(1*6)=50
50 % 10 = 0
So 3321-06-0 is a valid CAS Registry Number.
InChI:InChI=1/C24H33NO3.ClH/c1-5-13-22(6-2)28-24(20-14-9-7-10-15-20,21-16-11-8-12-17-21)23(26)27-19-18-25(3)4;/h7-12,14-17,22H,5-6,13,18-19H2,1-4H3;1H

3321-06-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(dimethylamino)ethyl 2-(2-ethylbutoxy)-2,2-diphenylacetate,hydrochloride

1.2 Other means of identification

Product number -
Other names UNII-2AFK8FCD4R

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:3321-06-0 SDS

3321-06-0Synthetic route

Denaverine hydrochloride
3321-06-0

Denaverine hydrochloride

A

2,2-diphenylacetic acid
117-34-0

2,2-diphenylacetic acid

B

Diphenylessigsaeure(2-dimethylaminoethyl)ester
2618-50-0

Diphenylessigsaeure(2-dimethylaminoethyl)ester

C

2-(dimethylamino)ethyl phenylglycolate
968-46-7

2-(dimethylamino)ethyl phenylglycolate

D

2-(2-Ethylbutoxy)-2,2-diphenylessigsaeure
2594-45-8

2-(2-Ethylbutoxy)-2,2-diphenylessigsaeure

E

Benzilic acid
76-93-7

Benzilic acid

Conditions
ConditionsYield
With hydrogenchloride In water Heating; hydrolysis; other reaction partner NaOH, other temperatures from room temp. to reflux, time from 10 min to 300 d;
Denaverine hydrochloride
3321-06-0

Denaverine hydrochloride

A

Diphenylessigsaeure(2-dimethylaminoethyl)ester
2618-50-0

Diphenylessigsaeure(2-dimethylaminoethyl)ester

B

Benzilic acid
76-93-7

Benzilic acid

C

3,3-Diphenylmorpholin-2-on
117516-86-6

3,3-Diphenylmorpholin-2-on

D

2-(2-Ethylbutoxy)diphenylessigsaureethylester
117545-06-9

2-(2-Ethylbutoxy)diphenylessigsaureethylester

E

2-(2-Ethylbutoxy)diphenylessigsauremethylester
91284-00-3

2-(2-Ethylbutoxy)diphenylessigsauremethylester

F

ethyl benzilate
52182-15-7

ethyl benzilate

Conditions
ConditionsYield
Product distribution; metabolism in the rat (oral application);
Denaverine hydrochloride
3321-06-0

Denaverine hydrochloride

A

2-(2-Ethylbutoxy)-2,2-diphenylessigsaeure
2594-45-8

2-(2-Ethylbutoxy)-2,2-diphenylessigsaeure

B

N-demethyl-1
117516-87-7

N-demethyl-1

C

2-<2-(2-ethylbutoxy)-2,2-diphenylacetoxy>acetic acid

2-<2-(2-ethylbutoxy)-2,2-diphenylacetoxy>acetic acid

D

2-(N-formyl-N-methylamino)ethyl O-(2-ethylbutyl)benzilate

2-(N-formyl-N-methylamino)ethyl O-(2-ethylbutyl)benzilate

E

C24H33NO4

C24H33NO4

Conditions
ConditionsYield
With 1H-imidazole; (porphirin)iron; dihydrogen peroxide In dichloromethane for 24h; Product distribution; Ambient temperature; comparison with aqueous system, with biological model systems: from rat livers of male Wistar rats; various catalysts, co-catalysts, O-donors;
Denaverine hydrochloride
3321-06-0

Denaverine hydrochloride

A

2-(2-Ethylbutoxy)-2,2-diphenylessigsaeure
2594-45-8

2-(2-Ethylbutoxy)-2,2-diphenylessigsaeure

B

N-demethyl-1
117516-87-7

N-demethyl-1

C

2-(N-formyl-N-methylamino)ethyl O-(2-ethylbutyl)benzilate

2-(N-formyl-N-methylamino)ethyl O-(2-ethylbutyl)benzilate

D

C24H33NO4

C24H33NO4

Conditions
ConditionsYield
With 1H-imidazole; (porphirin)iron for 24h; Ambient temperature;
Denaverine hydrochloride
3321-06-0

Denaverine hydrochloride

A

benzophenone
119-61-9

benzophenone

B

2-Hydroxybenzophenone
117-99-7

2-Hydroxybenzophenone

C

methyl benzilate
76-89-1

methyl benzilate

D

2-(2-Ethylbutoxy)diphenylessigsauremethylester
91284-00-3

2-(2-Ethylbutoxy)diphenylessigsauremethylester

E

2-(N-formyl-N-methylamino)ethyl O-(2-ethylbutyl)benzilate

2-(N-formyl-N-methylamino)ethyl O-(2-ethylbutyl)benzilate

F

2-(dimethylamino)ethyl O-(2-ethylbutyl)-2-hydroxybenzilate

2-(dimethylamino)ethyl O-(2-ethylbutyl)-2-hydroxybenzilate

G

other products found in nonaqueous system

other products found in nonaqueous system

Conditions
ConditionsYield
With 1H-imidazole; (porphirin)iron; dihydrogen peroxide In water for 24h; Product distribution; Ambient temperature; comparison with noaqueous system, with biological model systems: from rat livers of male Wistar rats; various catalysts;

3321-06-0Upstream product

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