Welcome to LookChem.com Sign In|Join Free

CAS

  • or

18450-73-2

Post Buying Request

18450-73-2 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

18450-73-2 Usage

Description

(R,R)-(+)-2,4-dimethylheptan-1-ol is a chiral alcohol with a molecular formula of C9H20O. It is characterized by a seven-carbon chain with two methyl groups and a hydroxyl group attached to the first carbon. (R,R)-(+)-2,4-dimethylheptan-1-ol is known for its fruity, floral odor and is widely utilized in various industries due to its unique properties.

Uses

Used in Pharmaceutical Industry:
(R,R)-(+)-2,4-dimethylheptan-1-ol is used as a chiral building block for the synthesis of various pharmaceuticals. Its unique structure allows for the creation of complex molecules with specific biological activities, making it a valuable component in drug development.
Used in Agrochemical Industry:
In the agrochemical industry, (R,R)-(+)-2,4-dimethylheptan-1-ol serves as a chiral building block for the synthesis of agrochemicals. Its ability to form specific molecular structures contributes to the development of targeted and effective products for agricultural applications.
Used in Fragrance and Flavor Industry:
(R,R)-(+)-2,4-dimethylheptan-1-ol is used as a key component in the production of flavors and fragrances for the cosmetic and food industries. Its fruity, floral odor makes it a desirable ingredient for creating pleasant and appealing scents.
Used in Chemical Processes:
(R,R)-(+)-2,4-dimethylheptan-1-ol is utilized as a solvent in various chemical processes. Its properties allow it to dissolve a wide range of substances, making it a versatile and useful compound in the chemical industry.
Used in Synthesis of Other Organic Compounds:
(R,R)-(+)-2,4-dimethylheptan-1-ol also serves as an intermediate in the synthesis of other organic compounds. Its unique structure and functional groups enable the creation of a diverse array of molecules for various applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 18450-73-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,4,5 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 18450-73:
(7*1)+(6*8)+(5*4)+(4*5)+(3*0)+(2*7)+(1*3)=112
112 % 10 = 2
So 18450-73-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H20O/c1-4-5-8(2)6-9(3)7-10/h8-10H,4-7H2,1-3H3/t8-,9-/m1/s1

18450-73-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,4R)-2,4-dimethylheptan-1-ol

1.2 Other means of identification

Product number -
Other names EINECS 242-335-7

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:18450-73-2 SDS

18450-73-2Relevant articles and documents

Synthesis of (2R,4R)-supellapyrone, the sex pheromone of the brownbanded cockroach, Supella longipalpa, and its three stereoisomers

Fujita, Ken,Mori, Kenji

, p. 493 - 502 (2007/10/03)

Supellapyrone [(2R,4R)-5-(2,4-dimethyl)-3-methyl-2H-pyran-2-one (1)], the female sex pheromone of the brownbanded cockroach (Supella longipalpa), and its three stereoisomers were synthesized by employing lipase-catalyzed desymmetrization or enantiomer separation of syn- or anti-2,4-dimethylpentane-1,5-diol (9) as the key step.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 18450-73-2