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113783-27-0

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113783-27-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113783-27-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,7,8 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 113783-27:
(8*1)+(7*1)+(6*3)+(5*7)+(4*8)+(3*3)+(2*2)+(1*7)=120
120 % 10 = 0
So 113783-27-0 is a valid CAS Registry Number.

113783-27-0SDS

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 1-(2-iodoethynyl)-2-nitrobenzene

1.2 Other means of identification

Product number -
Other names 1-iodoethynyl-2-nitrobenzene

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:113783-27-0 SDS

113783-27-0Downstream Products

113783-27-0Relevant articles and documents

Catalytic asymmetric formal [3+2] cycloaddition of isatogens with azlactones to construct indolin-3-one derivatives

Xie, Lihua,Li, Yi,Dong, Shunxi,Feng, Xiaoming,Liu, Xiaohua

, p. 239 - 242 (2021/01/14)

The chiral amide-guanidine-catalyzed asymmetric formal [3+2] cycloaddition of isatogens with azlactones is presented. This strategy provided a facile and feasible route to chiral indolin-3-one derivatives bearing two contiguous tetrasubstituted stereocent

Mild and efficient oxy-iodination of alkynes and phenols with potassium iodide and tert-butyl hydroperoxide

Rajender Reddy,Venkateshwar,Uma Maheswari,Santhosh Kumar

supporting information; experimental part, p. 2170 - 2173 (2010/06/14)

An efficient synthesis of 1-iodoalkynes and iodophenols was easily achieved by employing simple KI and TBHP. The reaction does not involve the use of a metal and base combination. A variety of substituted alkynes and phenols were prepared with good to excellent yield.

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