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lacinilene C 7-methyl ether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56362-72-2

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56362-72-2 Usage

Synthesis Reference(s)

Tetrahedron Letters, 19, p. 3993, 1978 DOI: 10.1016/S0040-4039(01)95120-2

Check Digit Verification of cas no

The CAS Registry Mumber 56362-72-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,3,6 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 56362-72:
(7*5)+(6*6)+(5*3)+(4*6)+(3*2)+(2*7)+(1*2)=132
132 % 10 = 2
So 56362-72-2 is a valid CAS Registry Number.
InChI:InChI=1/C16H20O3/c1-9(2)11-7-15(17)16(4,18)13-8-14(19-5)10(3)6-12(11)13/h6-9,18H,1-5H3/t16-/m1/s1

56362-72-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (+)-lacinilene C methyl ether

1.2 Other means of identification

Product number -
Other names Lacinilene C 7-methyl ether

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:56362-72-2 SDS

56362-72-2Relevant academic research and scientific papers

Catalytic asymmetric hydroxylative dearomatization of 2-naphthols: Synthesis of lacinilene derivatives

Zhang, Yu,Liao, Yuting,Liu, Xiaohua,Xu, Xi,Lin, Lili,Feng, Xiaoming

, p. 6645 - 6649 (2017/08/29)

An enantioselective hydroxylative dearomatization of 2-naphthols with oxaziridines has been accomplished using a N,N′-dioxide-scandium(iii) complex catalyst. Various substituted ortho-quinols could be obtained in high yields (up to 99%) and enantioselectivities (up to 95:5 er). This methodology could be applied in the synthesis of bioactive lacinilenes in a gram-scale reaction. Based on the experimental investigations and previous work, a possible catalytic model was proposed.

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