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N-tritylleucine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

32225-38-0

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32225-38-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32225-38-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,2,2 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 32225-38:
(7*3)+(6*2)+(5*2)+(4*2)+(3*5)+(2*3)+(1*8)=80
80 % 10 = 0
So 32225-38-0 is a valid CAS Registry Number.

32225-38-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-trityl-L-alanine,diethylamine salt

1.2 Other means of identification

Product number -
Other names N-Trityl-L-leucin

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:32225-38-0 SDS

32225-38-0Relevant academic research and scientific papers

A Synthesis of D-erythro- And L-threo-Sphingosine and Sphinganine Diastereomers via the Biomimetic Precursor 3-Ketosphinganine

Hoffman, Robert V.,Tao, Junhua

, p. 3979 - 3985 (2007/10/03)

The four stereoisomers of sphingosine and sphinganine can be produced in protected form by a short, convergent, biomimetic synthesis from serine. Yields are good (26-38% overall from commercially available serine derivatives), and the stereoselectivities are excellent (>92% de, >95% ee). Several sphingosine L-threo-sphingosine analogues with modified, functionalized tails were prepared to demonstrate the versatility of the method.

Efficient Synthesis of N-Triphenylmethyl α-Amino Acids

Mutter, Manfred,Hersperger, Rene

, p. 198 - 200 (2007/10/02)

A new one-pot synthesis of N-triphenylmethyl(trityl) α-amino acids 3 via their trityl ester 2 has been developed.

Efficient "One-Pot" Synthesis of N-Trityl Amino Acids

Barlos, Kleomenis,Papaioannou, Dionysios,Theodoropoulos, Dimitrios

, p. 1324 - 1326 (2007/10/02)

A sequential procedure has been developed whereby neutral amino acids 1 were tritylated via their corresponding trimethylsilyl esters 2 to afford, after mild hydrolysis, N-trityl amino acids 3 in high yields and purity.Hydroxy amino acids 4 were preferent

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