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133008-08-9

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133008-08-9 Usage

General Description

(R)-2,2-DIMETHYL-1,3-DIOXOLANE-4-PROPANOL is a chemical compound with the molecular formula C9H18O2. It is a colorless liquid that is used as a solvent in various industrial applications. (R)-2,2-DIMETHYL-1,3-DIOXOLANE-4-PROPANOL is also known for its use as a chiral resolving agent in organic synthesis. It is considered to be a versatile compound due to its ability to form stable complexes with various organic molecules. Additionally, it is known for its low toxicity and high stability, making it a popular choice for use in the pharmaceutical and chemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 133008-08-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,0,0 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 133008-08:
(8*1)+(7*3)+(6*3)+(5*0)+(4*0)+(3*8)+(2*0)+(1*8)=79
79 % 10 = 9
So 133008-08-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O3/c1-8(2)10-6-7(11-8)4-3-5-9/h7,9H,3-6H2,1-2H3/t7-/m1/s1

133008-08-9SDS

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 3-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]propan-1-ol

1.2 Other means of identification

Product number -
Other names -

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:133008-08-9 SDS

133008-08-9Relevant articles and documents

Reductive spiroannulation of nitriles with secondary electrophiles

Morin, Matthew D.,Rychnovsky, Scott D.

, p. 2051 - 2053 (2005)

(Chemical Equation Presented) The scope of reductive decyanation and spiroannulation reactions has been expanded to include secondary electrophiles for potentially useful transformations. Secondary phosphates and chlorides, as well as terminal epoxides, c

One-pot, two-step synthesis of unnatural α-amino acids involving the exhaustive aerobic oxidation of 1,2-diols

Inada, Haruki,Furukawa, Keisuke,Shibuya, Masatoshi,Yamamoto, Yoshihiko

, p. 15105 - 15108 (2019/12/26)

Herein, we report the nor-AZADO-catalyzed exhaustive aerobic oxidations of 1,2-diols to α-keto acids. Combining oxidation with transamination using dl-2-phenylglycine led to the synthesis of free α-amino acids (AAs) in one pot. This method enables the rapid and flexible preparation of a variety of valuable unnatural AAs, such as fluorescent AAs, photoactivatable AAs, and other functional AAs for bioorthogonal reactions.

Unified total synthesis of pteriatoxins and their diastereomers

Matsuura, Fumiyoshi,Peters, Rene,Anada, Masahiro,Harried, Scott S.,Hao, Junliang,Kishi, Yoshito

, p. 7463 - 7465 (2007/10/03)

A unified total synthesis is reported to access all of the possible diastereomers of pteriatoxins A-C, with the use of an intramolecular Diels-Alder reaction as the key step to form the carbo-macrocyclic core structure. The C34/C35-diol protecting groups were found to have significant effects on both the exo/endo-selectivity and the exo-facial selectivity of the intramolecular Diels-Alder process. Copyright

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