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2,2'-Binaphthalene, 1,1',8,8'-tetramethoxy-6,6'-dimethylis a chiral chemical compound belonging to the binaphthyl family, characterized by the molecular formula C32H30O4. It is renowned for its ability to induce high enantioselectivity in various chemical reactions, which is attributed to its unique structure featuring four methoxy groups and two methyl groups on the binaphthalene core. 2,2'-Binaphthalene, 1,1',8,8'-tetramethoxy-6,6'-dimethylserves as an essential chiral ligand in asymmetric catalysis, playing a crucial role in the development of pharmaceuticals, agrochemicals, and other fine chemicals due to its capacity to control the stereochemistry of reaction products.

17667-24-2

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17667-24-2 Usage

Uses

Used in Pharmaceutical Industry:
2,2'-Binaphthalene, 1,1',8,8'-tetramethoxy-6,6'-dimethylis utilized as a chiral ligand in asymmetric catalysis for the synthesis of enantiomerically pure pharmaceutical compounds. Its high enantioselectivity ensures the production of the desired enantiomer, which is crucial for the biological activity and safety of the final drug product.
Used in Agrochemical Industry:
In the agrochemical sector, 2,2'-Binaphthalene, 1,1',8,8'-tetramethoxy-6,6'-dimethylis employed as a chiral ligand to facilitate the enantioselective synthesis of agrochemicals with improved efficacy and reduced environmental impact. The precise control over stereochemistry allows for the development of more effective and targeted agrochemicals.
Used in Fine Chemicals Industry:
2,2'-Binaphthalene, 1,1',8,8'-tetramethoxy-6,6'-dimethylis also used as a chiral ligand in the synthesis of various fine chemicals, including fragrances, flavors, and specialty chemicals. Its ability to induce high enantioselectivity ensures the production of enantiomerically pure compounds with desired properties and applications.
Overall, 2,2'-Binaphthalene, 1,1',8,8'-tetramethoxy-6,6'-dimethylis a versatile and valuable reagent in the field of organic synthesis, particularly in asymmetric catalysis, due to its unique structure and properties that enable precise control over the stereochemistry of reaction products.

Check Digit Verification of cas no

The CAS Registry Mumber 17667-24-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,6 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17667-24:
(7*1)+(6*7)+(5*6)+(4*6)+(3*7)+(2*2)+(1*4)=132
132 % 10 = 2
So 17667-24-2 is a valid CAS Registry Number.

17667-24-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1,8-dimethoxy-6-methylnaphthalen-2-yl)-1,8-dimethoxy-6-methylnaphthalene

1.2 Other means of identification

Product number -
Other names 2,2'-Binaphthalene,1,1',8,8'-tetramethoxy-6,6'-dimethyl

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:17667-24-2 SDS

17667-24-2Upstream product

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