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745783-80-6

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745783-80-6 Usage

General Description

(R)-(-)-1-Indanyl isocyanate is a chemical compound with the molecular formula C10H7NO and a molecular weight of 157.17 g/mol. It is an isocyanate derivative with a chiral center, resulting in two stereoisomers. (R)-(-)-1-INDANYL ISOCYANATE is commonly used in organic synthesis as a reagent in the formation of isocyanate-containing compounds, such as polyurethanes and biologically active compounds. It is also used in the production of pharmaceuticals and agrochemicals. (R)-(-)-1-Indanyl isocyanate is a highly reactive and potentially hazardous compound, and precautions should be taken when handling and working with it.

Check Digit Verification of cas no

The CAS Registry Mumber 745783-80-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,5,7,8 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 745783-80:
(8*7)+(7*4)+(6*5)+(5*7)+(4*8)+(3*3)+(2*8)+(1*0)=206
206 % 10 = 6
So 745783-80-6 is a valid CAS Registry Number.

745783-80-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R)-1-isocyanato-2,3-dihydro-1H-indene

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:745783-80-6 SDS

745783-80-6Downstream Products

745783-80-6Relevant articles and documents

Enantioselective Aza-Henry reaction with an N-sulfinyl urea organocatalyst

Robak, Maryann T.,Trincado, Monica,Ellman, Jonathan A.

, p. 15110 - 15111 (2008/09/18)

A new class of organocatalyst has been developed that incorporates a sulfinyl group as a urea or thiourea substituent. The sulfinyl group serves to simultaneously acidify the urea and provide asymmetric induction in hydrogen-bond-catalyzed reactions. The utility of this new catalyst structure is demonstrated by the high selectivity provided in the aza-Henry reaction not only for aromatic N-Boc imine substrates but also for aliphatic imines for which enantioselective H-bonding catalysis has not previously been demonstrated. Copyright

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