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3-deoxy-1,2-O-isopropylidene-α-D-ribofuranose is a chemical compound derived from D-ribose, a naturally occurring sugar. It is characterized by the absence of an oxygen atom at the third carbon position, hence the term "3-deoxy." The compound features an isopropylidene group, which is a chemical structure consisting of two carbon atoms bonded to a central oxygen atom, protecting the 1,2-diol group. This modification is often used in organic synthesis to protect hydroxyl groups from unwanted reactions. The α-D-ribofuranose refers to the specific stereochemistry and ring structure of the sugar, with the hydroxyl group at the 2nd carbon in the alpha configuration. 3-deoxy-1,2-O-isopropylidene-α-D-ribofuranose is significant in the field of organic chemistry, particularly in the synthesis of complex carbohydrates and nucleosides, due to its ability to serve as a building block for more complex molecules.

3396-71-2

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3396-71-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3396-71-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,9 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3396-71:
(6*3)+(5*3)+(4*9)+(3*6)+(2*7)+(1*1)=102
102 % 10 = 2
So 3396-71-2 is a valid CAS Registry Number.

3396-71-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-deoxy-1,2-O-isopropylidene-α-D-erythro-pentofuranose

1.2 Other means of identification

Product number -
Other names ((3aR,5S,6aR)-2,2-dimethyl-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl)methanol

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:3396-71-2 SDS

3396-71-2Downstream Products

3396-71-2Relevant academic research and scientific papers

Generation of a low-valent titanium species from titanatrane and its catalytic reactions: Radical ring opening of oxetanes

Takekoshi, Naoto,Miyashita, Kenji,Shoji, Noriaki,Okamoto, Sentaro

supporting information, p. 2151 - 2157 (2013/10/01)

Treatment of a titanatrane complex with trimethylsilyl chloride and magnesium powder in tetrahydrofuran generated a low-valent titanium species. This species catalyzed the radical ring opening of epoxides and oxetanes to produce the corresponding less substituted alcohols. The reagent also catalyzed the deallylation and depropargylation of allylic and propargylic ethers, respectively, to provide the parent alcohols.

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