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51529-97-6

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51529-97-6 Usage

General Description

5,6,7,8-Tetrahydronaphthalene-2-carboxaldehyde, also known as 2-tetralone, is an organic compound that belongs to the class of cyclohexenyl compounds. Structurally, it is a derivative of tetralin, a compound composed of a fused ring system, where an aldehyde functional group attached at the 2-position. In its pure form, it appears as a clear light yellow liquid. It's used in a range of applications, including pharmaceuticals, as an intermediate in organic synthesis, and in the fragrance industry due to its sweet, woody scent. Its molecular formula is C11H12O, and it needs to be handled with care due to its flammable and irritant nature.

Check Digit Verification of cas no

The CAS Registry Mumber 51529-97-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,5,2 and 9 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 51529-97:
(7*5)+(6*1)+(5*5)+(4*2)+(3*9)+(2*9)+(1*7)=126
126 % 10 = 6
So 51529-97-6 is a valid CAS Registry Number.

51529-97-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6,7,8-tetrahydronaphthalene-2-carbaldehyde

1.2 Other means of identification

Product number -
Other names 5,6,7,8-Tetrahydro-naphthalene-2-carbaldehyde

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:51529-97-6 SDS

51529-97-6Relevant articles and documents

BCL-2 INHIBITOR

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Paragraph 0506-0508, (2021/10/22)

Disclosed herein is a compound of Formula (I) for inhibiting both Bcl-2 wild type and mutated Bcl-2, in particular, Bcl-2 G101V and D103Y, and a method of using the compound disclosed herein for treating dysregulated apoptotic diseases.

BI-CYCLO ALDEHYDE AS PERFUMING INGREDIENT

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Page/Page column 11-12, (2015/01/16)

The present invention relates to the field of perfumery and concerns some bi-cyclo derivative of formula (I), wherein R1 represents a hydrogen atom or a C1-2 alkyl group; R2 represents a hydrogen atom or a methyl group; and A represents a group of formula C3-5 alkanediyl group; at least one of said R1 or R2 represents a group containing at least one carbon atom; and said compound being in the form of a E or Z isomer or of a mixture thereof. Said compounds are valuable perfuming ingredients capable of imparting lily of the valley and citrus notes.

Synthesis of aromatic aldehydes by organocatalytic [4+2] and [3+3] cycloaddition of α,β-unsaturated aldehydes

Hong, Bor-Cherng,Tseng, Hsing-Chang,Chen, Shang-Hung

, p. 2840 - 2850 (2007/10/03)

Organocatalytic inter- and intramolecular [4+2] and [3+3] cycloadditions of α,β-unsaturated aldehydes to give polysubstituted aromatic aldehydes are described. High periselectivity for the cycloadditions, with catalyst effects exerted by l-proline and pyrrolidine-HOAc, as well as cocatalyst, additive effects, has been observed.

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