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8a-ethyl-3,4,8,8a-tetrahydronaphthalene-1,6(2H,7H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16154-18-0

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16154-18-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16154-18-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,5 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 16154-18:
(7*1)+(6*6)+(5*1)+(4*5)+(3*4)+(2*1)+(1*8)=90
90 % 10 = 0
So 16154-18-0 is a valid CAS Registry Number.

16154-18-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 8a-ethyl-3,4,7,8-tetrahydro-2H-naphthalene-1,6-dione

1.2 Other means of identification

Product number -
Other names 8a-ethyl-3,4,8,8a-tetrahydronaphthalene-1,6(2h,7h)-dione

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:16154-18-0 SDS

16154-18-0Downstream Products

16154-18-0Relevant academic research and scientific papers

Prolinamide/PPTS-catalyzed Hajos-Parrish annulation: Efficient approach to the tricyclic core of cylindricine-type alkaloids

Zhang, Xiao-Ming,Wang, Min,Tu, Yong-Qiang,Fan, Chun-An,Jiang, Yi-Jun,Zhang, Shu-Yu,Zhang, Fu-Min

scheme or table, p. 2831 - 2835 (2009/05/07)

A series of Wieland-Miescher ketone analogues bearing highly functionalized substituents are efficiently constructed in high enantioselectivities and good yields using catalytic amounts of prolinamide and PPTS. We have successfully utilized this reaction as a key step to synthesize the tricyclic core of cylindricine type alkaloids. Georg Thieme Verlag Stuttgart.

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