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180690-93-1

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180690-93-1 Usage

General Description

(2-Formyl-6-Methoxy-Phenyl)-Carbamic Acid Tert-Butyl Ester is a chemical compound with the molecular formula C13H17NO4. It is a carbamic acid ester, which is commonly used as a reagent in organic synthesis. (2-FORMYL-6-METHOXY-PHENYL)-CARBAMIC ACID TERT-BUTYL ESTER is often utilized in pharmaceutical and agrochemical research due to its ability to form various derivatives and functional groups. Additionally, it can also act as a precursor for the synthesis of other bioactive molecules. The tert-butyl ester group provides stability and protection to the carbamic acid, making it a versatile and useful compound in chemical research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 180690-93-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,6,9 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 180690-93:
(8*1)+(7*8)+(6*0)+(5*6)+(4*9)+(3*0)+(2*9)+(1*3)=151
151 % 10 = 1
So 180690-93-1 is a valid CAS Registry Number.

180690-93-1 Well-known Company Product Price

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  • Aldrich

  • (JWP00352)  (2-Formyl-6-methoxy-phenyl)-carbamic acid tert-butyl ester  AldrichCPR

  • 180690-93-1

  • JWP00352-1G

  • 9,342.45CNY

  • Detail

180690-93-1SDS

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 tert-butyl 2-formyl-6-methoxyphenylcarbamate

1.2 Other means of identification

Product number -
Other names (2-Formyl-6-methoxy-phenyl)-carbamic acid tert-butyl ester

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:180690-93-1 SDS

180690-93-1Relevant articles and documents

Chiral relay effect: 4-substituted 1,3-benzoxazol-2-(3H)-ones as achiral templates for enantioselective Diels-Alder reactions

Quaranta, Laura,Corminboeuf, Olivier,Renaud, Philippe

, p. 39 - 41 (2007/10/03)

(matrix presented) A new strategy to control the enantioselectivity of Lewis acid catalyzed reactions has been investigated. The use of N-acryloyl-1,3-benzoxazol-2-(3H)-ones substituted at position 4 leads to the formation of diastereomeric complexes as a

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