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(2R)-1,4,5,6-tetrachlorobicyclo[2.2.1]hept-5-en-2-ol is a tetrachlorinated derivative of bicyclo[2.2.1]hept-5-en-2-ol, a bicyclic organic compound and a chlorinated alcohol. As the (R)-enantiomer, it possesses a specific spatial arrangement of its atoms, which may contribute to its unique properties and potential applications.

90254-10-7

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90254-10-7 Usage

Uses

Used in Chemical Reactions:
(2R)-1,4,5,6-tetrachlorobicyclo[2.2.1]hept-5-en-2-ol is used as a building block in organic synthesis for various chemical reactions due to its unique structure and reactivity.
Used in Pharmaceutical Industry:
(2R)-1,4,5,6-tetrachlorobicyclo[2.2.1]hept-5-en-2-ol is used as a potential candidate in pharmaceuticals for its specific properties, making it valuable for researchers in drug discovery and development.
Used in Materials Science:
(2R)-1,4,5,6-tetrachlorobicyclo[2.2.1]hept-5-en-2-ol is used in materials science for its potential applications in the development of new materials with unique properties, such as improved stability or reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 90254-10-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,2,5 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 90254-10:
(7*9)+(6*0)+(5*2)+(4*5)+(3*4)+(2*1)+(1*0)=107
107 % 10 = 7
So 90254-10-7 is a valid CAS Registry Number.

90254-10-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (5R)-1,2,3,4-tetrachlorobicyclo[2.2.1]hept-2-en-5-ol

1.2 Other means of identification

Product number -
Other names 2-Ethylamino-1-phenylpropanol

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:90254-10-7 SDS

90254-10-7Downstream Products

90254-10-7Relevant academic research and scientific papers

ENZYMATIC ACYLATION USING ACID ANHYDRIDES: CRUCIAL REMOVAL OF ACID

Berger, B.,Rabiller, C. G.,Koenigsberger, K.,Faber, K.,Griengl, H.

, p. 541 - 546 (2007/10/02)

An efficient enzymatic resolution of 7,7-disubstituted 1,4,5,6-tetrachlorobicyclohept-5-en-2-ols was accomplished by means of lipase AY-30 from Candida cylindracea in toluene.When acid anhydrides were used as acyl donors, the enantioselectivity was found to depend strongly on the reaction conditions: Whereas low selectivity (E 200).Alternatively, adsorption of the biocatalyst onto Celite was equally effective (E >300).Complete specificity was obtained when vinyl acetate was used as acyl donor (E ca.1000).

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