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121734-64-3

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121734-64-3 Usage

General Description

1-Benzo[1,3]dioxol-5-yl-ethylamine, also known as safrole, is a chemical compound commonly found in plants such as Sassafras albidum. It is a colorless to pale yellow liquid with a slightly sweet and spicy odor. Safrole has been used in the production of fragrances, soaps, and flavorings, and has also been used in traditional medicine for its purported stimulant and aphrodisiac properties. However, safrole is also a precursor for the illicit production of MDMA (ecstasy), and its use as a food additive has been banned in the United States and Europe due to its potential carcinogenic properties. Research has also shown that safrole can cause hepatocellular carcinoma in rats, leading to further concerns about its safety and utilization in consumer products.

Check Digit Verification of cas no

The CAS Registry Mumber 121734-64-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,7,3 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 121734-64:
(8*1)+(7*2)+(6*1)+(5*7)+(4*3)+(3*4)+(2*6)+(1*4)=103
103 % 10 = 3
So 121734-64-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO2/c1-6(10)7-2-3-8-9(4-7)12-5-11-8/h2-4,6H,5,10H2,1H3

121734-64-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1,3-benzodioxol-5-yl)ethanamine

1.2 Other means of identification

Product number -
Other names 1-(3,4-methylenedioxyphenyl)ethylamine

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:121734-64-3 SDS

121734-64-3Relevant articles and documents

BAX INHIBITORS AND USES THEREOF

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Paragraph 00262, (2021/01/23)

A compound having formula (I) or (II) for use inhibiting Bax mediated cell death and/or apoptosis.

Method for preparing primary amine by catalyzing reductive amination of aldehyde ketone compounds

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Paragraph 0066-0067, (2020/05/30)

The invention discloses a method for preparing primary amine by catalyzing reductive amination of aldehyde ketone compounds. The method comprises the following steps: 1) mixing nickel nitrate hexahydrate, citric acid and an organic solvent, carrying out heating and stirring until a colloidal material is obtained, drying the colloidal material, roasting the colloidal material in a protective atmosphere, pickling, washing and drying a roasted product, and performing a partial oxidation reaction on a dried product in an oxygen-nitrogen mixed atmosphere to obtain a catalyst for a reductive amination reaction; and 2) mixing aldehyde or ketone compounds, a methanol solution of ammonia and the reductive amination reaction catalyst, introducing hydrogen, and carrying out a reductive amination reaction. The method has the advantages of high primary amine yield, high selectivity, wide aldehyde ketone substrate range, short reaction time, mild reaction conditions, low cost, greenness, economicalperformance and the like; the used reductive amination reaction catalyst can be recycled more than 10 times, and the catalytic activity of the catalyst is not obviously changed in gram-level reactions; and the method is suitable for large-scale application.

METHOD FOR THE HOMOGENEOUS CATALYTIC REDUCTIVE AMINATION OF CARBONYL COMPOUNDS

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Paragraph 0212; 0219-0221, (2018/07/29)

The present invention relates to a method for the reductive amination of a carbonyl compound, comprising one or more carbonyl groups amenable to reductive amination, forming the corresponding primary amine, characterized in that the reaction is carried out in the presence of a homogeneously dissolved catalyst complex K, comprising at least one metal atom from Group 8, 9 or 10 of the periodic table, bearing a bidentate phosphane ligand, a carbonyl ligand, a neutral ligand and a hydride ligand, and also an acid as co-catalyst.

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