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29700-34-3

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29700-34-3 Usage

Chemical Properties

Solid

Uses

L-[15N]Phenylalanine is an isotopically labeled analog of L_Phenylalanine (P319415), which is an essential amino acid. L-[15N]Phenylalanine is used as a genetic tool for selectively labeling proteins.

Check Digit Verification of cas no

The CAS Registry Mumber 29700-34-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,7,0 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 29700-34:
(7*2)+(6*9)+(5*7)+(4*0)+(3*0)+(2*3)+(1*4)=113
113 % 10 = 3
So 29700-34-3 is a valid CAS Registry Number.

29700-34-3 Well-known Company Product Price

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  • Aldrich

  • (490105)  L-Phenylalanine-15N  98 atom % 15N

  • 29700-34-3

  • 490105-500MG

  • 5,243.94CNY

  • Detail

29700-34-3SDS

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 L-Phenylalanine-15N

1.2 Other means of identification

Product number -
Other names L-<15N>phenylalanine

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:29700-34-3 SDS

29700-34-3Upstream product

29700-34-3Downstream Products

29700-34-3Relevant articles and documents

Stereoselective synthesis of stable isotope-labeled L-α-amino acids: Electrophilic amination of oppolzer's acyl sultams in the synthesis of L-[15N]alanine, L-[15N]valine, L-[15N]leucine, L-[15N]phenylalanine and

Lodwig,Unkefer

, p. 239 - 248 (2007/10/03)

Using 1-chloro-1-[15N]nitrosocyclohexane, we have prepared five L-[α-15N]amino acids. The stereoselective electophillic hydroxyamination of (S)-acylbornane-10,2-sultams, followed by Zn(o)/H+ reduction, and alkaline cleavag

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