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5471-56-7

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5471-56-7 Usage

General Description

1-(cyclohex-1-en-1-yl)propan-2-amine is a chemical compound with the molecular formula C10H17N. It is an amine derivative, containing a cyclohexene ring and a propan-2-amine group. 1-(cyclohex-1-en-1-yl)propan-2-amine is used in organic synthesis and pharmaceutical research. It may also have potential applications in the development of new drugs or as a building block for the synthesis of other chemical compounds. The compound's structure and properties make it a valuable target for studying its reactivity and potential biological activity. Overall, 1-(cyclohex-1-en-1-yl)propan-2-amine is a versatile chemical with various potential uses in the field of chemistry and pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 5471-56-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,7 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5471-56:
(6*5)+(5*4)+(4*7)+(3*1)+(2*5)+(1*6)=97
97 % 10 = 7
So 5471-56-7 is a valid CAS Registry Number.

5471-56-7SDS

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 1-(cyclohexen-1-yl)propan-2-amine

1.2 Other means of identification

Product number -
Other names 2-cyclohex-1-enyl-1-methyl-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:5471-56-7 SDS

5471-56-7Downstream Products

5471-56-7Relevant articles and documents

Catalytic Multisite-Selective Acetoxylation Reactions at sp2 vs sp3 C-H Bonds in Cyclic Olefins

Zang, Zhong-Lin,Zhao, Sheng,Karnakanti, Shuklachary,Liu, Cheng-Lin,Shao, Pan-Lin,He, Yun

supporting information, p. 5014 - 5017 (2016/10/14)

The first Pd-catalyzed multisite-selective acetoxylation reactions are disclosed at an unactivated alkene sp2 C-H bond versus secondary allylic sp3 C-H bond in cyclic olefins via the modulation of directing groups. The different directing groups overcome the key challenge in differentiating C-H bonds and provide a new controlling approach for site-specific C-H activation. A wide variety of substrates are readily acetoxylated under operationally simple conditions. Mechanistic studies suggest that different Pd (IV) intermediates were involved in the multisite-selective acetoxylation reactions.

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