6705-89-1 Usage
Structure
Cyclic acetal of two dioxolane rings connected by a central carbon atom
The compound is formed by two five-membered dioxolane rings (a type of ether with two oxygen atoms) linked together by a single carbon atom.
Usage
Solvent or precursor in organic synthesis reactions
2,2'-Bi(1,3-dioxolane) is commonly used as a solvent for various chemical reactions or as a starting material to produce other compounds in organic synthesis.
Color
Colorless
The liquid form of 2,2'-Bi(1,3-dioxolane) is colorless and transparent.
State
Volatile liquid
As a volatile liquid, 2,2'-Bi(1,3-dioxolane) easily evaporates at room temperature, producing vapors.
Boiling point
High
The compound has a high boiling point, making it suitable for use in various chemical processes that require heating.
Melting point
Low
2,2'-Bi(1,3-dioxolane) has a low melting point, which means it turns into a liquid at relatively low temperatures.
Hazard class
Moderately hazardous
2,2'-Bi(1,3-dioxolane) is considered to be moderately hazardous, and appropriate safety measures should be taken when handling and storing it.
Handling and storage precautions
Use personal protective equipment (PPE) when handling the compound.
Store in a cool, dry, and well-ventilated area, away from direct sunlight and heat sources.
Keep away from incompatible substances and potential sources of ignition.
Follow local and international regulations and guidelines for the safe handling and disposal of hazardous chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 6705-89-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,0 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6705-89:
(6*6)+(5*7)+(4*0)+(3*5)+(2*8)+(1*9)=111
111 % 10 = 1
So 6705-89-1 is a valid CAS Registry Number.
6705-89-1Relevant articles and documents
A Convenient Synthesis of Substituted Polyether Diols
Castro, Peter P.,Tihomirov, Serge,Gutierrez, Carlos G.
, p. 5179 - 5181 (2007/10/02)
Alkyl-substituted polyether diols (or polythioether diols), which are potential precursors to substituted crown ethers, are produced in high yield by the selective reductive cleavage of C-O bonds in bis(cyclic acetals) by borane or monochloroborane.
