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92573-86-9

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92573-86-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92573-86-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,5,7 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 92573-86:
(7*9)+(6*2)+(5*5)+(4*7)+(3*3)+(2*8)+(1*6)=159
159 % 10 = 9
So 92573-86-9 is a valid CAS Registry Number.

92573-86-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(2E)-3-phenylprop-2-en-1-yl]aniline

1.2 Other means of identification

Product number -
Other names phenyl-(3-phenylallyl)-amine

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:92573-86-9 SDS

92573-86-9Relevant articles and documents

Azetadiene iron carbonyl compounds and their preparation and application

-

Paragraph 0102-0104, (2022/01/20)

The present invention discloses the structure of two novel azerodiene iron carbonyl compounds having a structure shown in formula (1): (R = adamantyl, 1-naphthyl), formula (1). The present invention discloses a method for preparing these two compounds: fi

Sulfated polyborate: A dual catalyst for the reductive amination of aldehydes and ketones by NaBH4

Ganwir, Prerna,Chaturbhuj, Ganesh

, (2021/05/19)

An efficient, quick, and environment-friendly one-pot reductive amination of aldehydes or ketones was developed. In ethanol at 70 °C, a imination catalyzed by sulfated polyborate and further reduced by sodium borohydride yields various amines. The present method has many significant benefits, including a shorter reaction time, excellent yields, and a hassle-free, straightforward experimental process. The reaction has a wide range of applications due to its flexibility, including secondary amine for reductive amination.

PH-Mediated Selective Synthesis of N-Allylic Alkylation or N-Alkylation Amines with Allylic Alcohols via an Iridium Catalyst in Water

Luo, Nianhua,Zhong, Yuhong,Shui, Hongling,Luo, Renshi

supporting information, p. 15509 - 15521 (2021/11/01)

Amination of allylic alcohols is an effective approach in the facile synthesis of N-allylic alkylation or N-alkylation amines. Recently, a series of catalysts were devised to push forward this transformation. However, current synthetic methods are typical

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