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Carbamic acid, [(2-methylphenyl)methylene]-, 1,1-dimethylethyl ester, [N(E)]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

743430-47-9

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743430-47-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 743430-47-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,3,4,3 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 743430-47:
(8*7)+(7*4)+(6*3)+(5*4)+(4*3)+(3*0)+(2*4)+(1*7)=149
149 % 10 = 9
So 743430-47-9 is a valid CAS Registry Number.

743430-47-9SDS

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 o-tolualdehyde N-(tert-butoxycarbonyl)imine

1.2 Other means of identification

Product number -
Other names [1-o-Tolyl-meth-(E)-ylidene]-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:743430-47-9 SDS

743430-47-9Relevant academic research and scientific papers

Versatile supramolecular copper(II) Complexes for Henry and Aza-Henry reactions

Zhang, Guoqi,Yashima, Eiji,Woggon, Wolf-D.

supporting information; scheme or table, p. 1255 - 1262 (2009/12/22)

Chiral supramolecular metal-organic frameworks assembled from copper complexes catalyse Henry and aza-Henry reactions of aromatic and aliphatic aldehydes and N-protected aromatic imines in high yield and good to excellent enantioselectivity. Reactions can

Asymmetric catalytic Mannich reactions catalyzed by urea derivatives: Enantioselective synthesis of β-aryl-β-amino acids

Wenzel, Anna G.,Jacobsen, Eric N.

, p. 12964 - 12965 (2007/10/03)

Highly enantioselective addition reactions between silyl ketene acetals and N-Boc aldimines are catalyzed by the thiourea-based catalyst 1c. Extraordinary scope is observed in this methodology with regard to the imine substrate, with aryl and heteroaromatic derivatives generally affording nearly quantitative yields of β-amino ester product in up to 98% enantioselectivity. Copyright

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