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FMOC-(R)-3-AMINO-3-(2-NAPHTHYL)-PROPIONIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

511272-48-3

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511272-48-3 Usage

Chemical Properties

White solid

Check Digit Verification of cas no

The CAS Registry Mumber 511272-48-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,1,2,7 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 511272-48:
(8*5)+(7*1)+(6*1)+(5*2)+(4*7)+(3*2)+(2*4)+(1*8)=113
113 % 10 = 3
So 511272-48-3 is a valid CAS Registry Number.

511272-48-3SDS

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 (3R)-3-(9H-fluoren-9-ylmethoxycarbonylamino)-3-naphthalen-2-ylpropanoic acid

1.2 Other means of identification

Product number -
Other names (R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(naphthalen-2-yl)propanoic acid

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:511272-48-3 SDS

511272-48-3Downstream Products

511272-48-3Relevant academic research and scientific papers

Catalytic asymmetric three-component synthesis of homoallylic amines

Gandhi, Shikha,List, Benjamin

supporting information, p. 2573 - 2576 (2013/04/10)

It takes three to make things go right: The first direct asymmetric three-component reaction of aldehydes, carbamates, and allyltrimethylsilane leading to enantioenriched homoallylic amines has been developed using a new chiral disulfonimide catalyst (see scheme). The method employs readily available, inexpensive, and nontoxic starting materials and is applicable to both aromatic and aliphatic aldehydes. Copyright

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