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(S)-2-O-Benzyl-1-iodo-3-butene, an organic compound, features a benzyl group attached to the carbon 2 position and an iodine atom at the carbon 1 position of a butene molecule. As a chiral compound, its (S)-configuration signifies that the highest priority groups are arranged in a counterclockwise direction around the chiral center. (S)-2-O-BENZYL-1-IODO-3-BUTENE is widely recognized for its utility as a building block in organic synthesis, allowing for the creation of more complex molecules through various chemical reactions. Furthermore, its potential applications extend to the pharmaceutical and agrochemical industries, where its versatile reactivity can be harnessed to produce biologically active substances.

124909-04-2

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124909-04-2 Usage

Uses

Used in Organic Synthesis:
(S)-2-O-Benzyl-1-iodo-3-butene is used as a key building block in the field of organic synthesis for the creation of more complex molecules. Its unique structure and reactivity make it a valuable component in the synthesis of various organic compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (S)-2-O-Benzyl-1-iodo-3-butene is utilized as a versatile intermediate for the development of biologically active substances. Its potential to form a wide range of complex molecules contributes to the discovery and synthesis of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
(S)-2-O-Benzyl-1-iodo-3-butene also finds application in the agrochemical industry, where it serves as a crucial intermediate in the synthesis of various agrochemical products. Its reactivity and structural diversity enable the development of new compounds with targeted biological activities, such as pesticides or plant growth regulators.

Check Digit Verification of cas no

The CAS Registry Mumber 124909-04-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,9,0 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 124909-04:
(8*1)+(7*2)+(6*4)+(5*9)+(4*0)+(3*9)+(2*0)+(1*4)=122
122 % 10 = 2
So 124909-04-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H13IO/c1-2-11(8-12)13-9-10-6-4-3-5-7-10/h2-7,11H,1,8-9H2/t11-/m0/s1

124909-04-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-2-O-BENZYL-1-IODO-3-BUTENE

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

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More Details:124909-04-2 SDS

124909-04-2Relevant academic research and scientific papers

SYNTHESIS OF (R)-2-BENZYLOXY-1-IODOD-3-BUTENE - A NEW CHIRAL SYNTHON FROM L-(+)-TARTARIC ACID : ITS APPLICATION TO (R)-ν-CAPROLACTONE

Yadav, J. S.,Rao, Sreenivasa E.,Rao, Sreenivasa V.

, p. 705 - 712 (2007/10/02)

A practical synthesis of (R)-2-benzyloxy-1-iodo-3-butene, a bifunctional chiral synthon from (R,R)-tartaric acid and its application to (R)-ν-caprolactone, a pheromone of Trogoderma species, is described.

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