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17155-65-6

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17155-65-6 Usage

Physical state

Colorless liquid

Odor

Pleasant

Flammability

Flammable

Uses

Solvent in various industrial applications, production of pharmaceuticals, pesticides, and other organic chemicals

Stability

Highly stable

Toxicity

Low toxicity

Safety precautions

Handle and store carefully, avoid exposure to high temperatures, sparks, or open flames to prevent combustion.

Check Digit Verification of cas no

The CAS Registry Mumber 17155-65-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,5 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17155-65:
(7*1)+(6*7)+(5*1)+(4*5)+(3*5)+(2*6)+(1*5)=106
106 % 10 = 6
So 17155-65-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H14O2/c1-3-6(2)7-8-4-5-9-7/h6-7H,3-5H2,1-2H3

17155-65-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-pentan-2-yl-1,3-dioxolane

1.2 Other means of identification

Product number -
Other names EINECS 241-212-5

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:17155-65-6 SDS

17155-65-6Downstream Products

17155-65-6Relevant articles and documents

Visible-light-induced acetalization of aldehydes with alcohols

Yi, Hong,Niu, Linbin,Wang, Shengchun,Liu, Tianyi,Singh, Atul K.,Lei, Aiwen

supporting information, p. 122 - 125 (2017/11/27)

In this work, we have achieved a simple and general method for acetalization of aldehydes by means of a photochemical reaction under low-energy visible light irradiation. A broad range of aromatic, heteroaromatic, and aliphatic aldehydes have been protected under neutral conditions in good to excellent yields using a catalytic amount of Eosin Y as the photocatalyst. Our visible light mediated acetalization strategies are successful for more challenging acid-sensitive aldehydes and sterically hindered aldehydes. Notably, this protocol is chemoselective to aldehydes, while ketones remain intact.

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