143170-07-4 Usage
Description
(2R,6R)-2,6-Heptanediol, with the molecular formula C7H16O2, is a colorless, odorless liquid that is soluble in water. It is a chiral compound with specific stereochemistry at the 2nd and 6th carbon atoms, which is crucial for its applications. This chemical is known for its versatility in the synthesis of various organic compounds and as a monomer for polymer production.
Uses
Used in Chemical Synthesis:
(2R,6R)-2,6-Heptanediol is used as a key intermediate in the synthesis of various organic compounds. Its unique stereochemistry allows for the creation of specific molecules with desired properties, making it valuable in the development of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Polymer Production:
As a monomer, (2R,6R)-2,6-Heptanediol is used in the production of polymers. Its incorporation into polymer chains can impart specific characteristics, such as improved mechanical properties or enhanced biodegradability, depending on the polymer's intended application.
Used in Cosmetic and Personal Care Industry:
(2R,6R)-2,6-Heptanediol is used as a moisturizing and conditioning agent in skin and hair care products. Its ability to retain moisture and improve the texture of hair and skin makes it a valuable ingredient in cosmetic formulations.
Used in Pharmaceutical Industry:
(2R,6R)-2,6-Heptanediol has potential applications in the pharmaceutical industry, where it may be used as an active ingredient or as a component in drug formulations. Its specific stereochemistry could be leveraged to develop targeted therapies or improve the efficacy of existing medications.
Used in Food Industry:
Although not extensively detailed in the provided materials, (2R,6R)-2,6-Heptanediol may have potential uses in the food industry, such as a flavoring agent or a component in food additives, given its solubility and compatibility with other ingredients.
Safety Precautions:
It is important to handle (2R,6R)-2,6-Heptanediol with caution, as it can be irritating to the skin, eyes, and respiratory tract. Proper safety measures, such as wearing protective gear and working in well-ventilated areas, should be taken to minimize exposure and potential health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 143170-07-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,1,7 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 143170-07:
(8*1)+(7*4)+(6*3)+(5*1)+(4*7)+(3*0)+(2*0)+(1*7)=94
94 % 10 = 4
So 143170-07-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H16O2/c1-6(8)4-3-5-7(2)9/h6-9H,3-5H2,1-2H3/t6-,7-/m1/s1
143170-07-4Relevant articles and documents
Lactols in Stereoselection 1. Highly selective 1,4- and 1,5-Asymmetric Induction
Tomooka, Katsuhiko,Okinaga, Tatsuyuki,Suzuki, Keisuke,Tsuchihashi, Gen-ichi
, p. 6335 - 6338 (2007/10/02)
Nucleophilic addition to substituted γ- and δ-lactols with titanium reagents provides 1,4-syn and 1,5-syn diols in high stereoselectivity, which represents a new and simple method for the remote asymmetric induction.
