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7500-75-6

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7500-75-6 Usage

General Description

[Bis(hexyloxy)methyl]benzene is a chemical compound consisting of a benzene ring with two adjacent, non-identical methylene group substituents, each linked to a hexyloxy group. [bis(hexyloxy)methyl]benzene is commonly used as a high boiling point solvent and as a plasticizer in various industries. It is also known for its use as an intermediate in the synthesis of other organic compounds. Moreover, due to its low toxicity and biodegradability, it is considered to be environmentally friendly. However, it is important to handle this chemical with care as it may cause irritation to the eyes, skin, and respiratory system, and should be stored and disposed of properly to prevent any adverse impact on human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 7500-75-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,0 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7500-75:
(6*7)+(5*5)+(4*0)+(3*0)+(2*7)+(1*5)=86
86 % 10 = 6
So 7500-75-6 is a valid CAS Registry Number.

7500-75-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name dihexoxymethylbenzene

1.2 Other means of identification

Product number -
Other names Dihexylacetalbenzaldehyd

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:7500-75-6 SDS

7500-75-6Downstream Products

7500-75-6Relevant articles and documents

Zn(ii) chloride-catalyzed direct coupling of various alkynes with acetals: Facile and inexpensive access to functionalized propargyl ethers

Suzuki, Itaru,Yasuda, Makoto,Baba, Akio

supporting information, p. 11620 - 11622 (2013/12/04)

The coupling of acetals with various alkynes was achieved using only 1 mol% of inexpensive and mild Lewis acid ZnCl2, which furnished propargyl ethers. The coupling was catalyzed by Zn(OMe)Cl, which was generated in situ to form an alkynylzinc species. This protocol was allowed to expand to a one-pot subsequent reaction with allylchlorosilane to obtain a 1,4-enyne product.

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