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5-(2-Aminopropyl)indole is an organic compound with the chemical formula C11H14N2. It is a derivative of indole, a heterocyclic aromatic organic compound, and features an aminopropyl group attached to the 5-position of the indole ring. This molecule is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as in the development of fluorescent probes and other specialty chemicals. Its unique structure allows for a range of chemical modifications, making it a versatile building block in organic synthesis.

3784-30-3

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3784-30-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3784-30-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,8 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3784-30:
(6*3)+(5*7)+(4*8)+(3*4)+(2*3)+(1*0)=103
103 % 10 = 3
So 3784-30-3 is a valid CAS Registry Number.

3784-30-3 Well-known Company Product Price

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  • Cerilliant

  • (A-107)  5-API (5-IT) solution  1.0 mg/mL in acetonitrile, ampule of 1 mL, certified reference material

  • 3784-30-3

  • A-107-1ML

  • 1,302.21CNY

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3784-30-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1H-indol-5-yl)propan-2-amine

1.2 Other means of identification

Product number -
Other names 5-API

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:3784-30-3 SDS

3784-30-3Synthetic route

5‐(2‐aminopropyl)indol
3784-30-3

5‐(2‐aminopropyl)indol

A

5‐(2‐aminopropyl)indol

5‐(2‐aminopropyl)indol

B

5‐(2‐aminopropyl)indol

5‐(2‐aminopropyl)indol

Conditions
ConditionsYield
With (2R,3R,11R,12R)-(+)-18-crown-6-2,3,11,12-tetracarbonic acid In aq. buffer at 20℃; for 0.25h; pH=2.1; Resolution of racemate; enantioselective reaction;
With Lux i-Amylose-1 column In hexane; diethylamine; isopropyl alcohol at 20℃; Resolution of racemate;
5‐(2‐aminopropyl)indol
3784-30-3

5‐(2‐aminopropyl)indol

C11H14N2

C11H14N2

C11H14N2

C11H14N2

Conditions
ConditionsYield
With β‐cyclodextrin In aq. phosphate buffer at 25℃; pH=2.5; Reagent/catalyst; Resolution of racemate;

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