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155566-54-4

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155566-54-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 155566-54-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,5,6 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 155566-54:
(8*1)+(7*5)+(6*5)+(5*5)+(4*6)+(3*6)+(2*5)+(1*4)=154
154 % 10 = 4
So 155566-54-4 is a valid CAS Registry Number.

155566-54-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,4-tetrahydro-1-naphthalenecarbaldehyde

1.2 Other means of identification

Product number -
Other names tetralin aldehyde

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:155566-54-4 SDS

155566-54-4Relevant articles and documents

Cobalt-Catalyzed Diborylation of 1,1-disubstituted Vinylarenes: A Practical Route to Branched gem-Bis(boryl)alkanes

Teo, Wei Jie,Ge, Shaozhong

, p. 1654 - 1658 (2018)

We report the first catalytic diborylation of 1,1-disubstituted vinylarenes with pinacolborane using a cobalt catalyst generated from bench-stable Co(acac)2 and xantphos. A wide range of 1,1-disubstituted vinylarenes underwent this transformati

Palladium-Catalyzed Allenamide Carbopalladation/Allylation with Active Methine Compounds

Zhu, Xiaoyi,Li, Ruibo,Yao, Hequan,Lin, Aijun

supporting information, p. 4630 - 4634 (2021/06/28)

A palladium-catalyzed allenamide carbopalladation/allylation with active methine compounds has been developed. Various indoles and isoquinolinones bearing a quaternary carbon center were achieved with good efficiency, a broad substrate scope and good functional group tolerance. This reaction underwent cascade oxidative addition, carbopalladation, and allylic alkylation, and two new C-C bonds were formed in one pot.

Synthesis and biological activity of both enantiomers of kujigamberol isolated from 85-million-years-old Kuji amber

Ye, Yue Qi,Koshino, Hiroyuki,Hashizume, Daisuke,Minamikawa, Yuki,Kimura, Ken-Ichi,Takahashi, Shunya

scheme or table, p. 4259 - 4262 (2012/09/22)

The full-structure of a norlabdane terpenoid, kujigamberol (1) was determined by total synthesis. Key features of the total synthesis are (1) installation of isopentyl group through an o-lithiation of benzamide, (2) construction of tetralone by the RCM reaction, and (3) optical resolution of (±)-1 using chromatographical separation of the corresponding camphanates. X-ray crystallographical analysis of p-bromobenzoate obtained from the more polar camphanate that was identical with a natural derivative, revealed natural kujigamberol to have an S-configuration. Both the natural enantiomer and its (R)-antipode showed the same inhibitory activity toward the mutant yeast and HL-60 cells, while simple analogs without alkyl groups at the C-8 and 9 positions of (±)-1 had no such activity.

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