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

7682-16-8

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7682-16-8 Usage

Uses

Substrate for aminoacylase

Check Digit Verification of cas no

The CAS Registry Mumber 7682-16-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,8 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7682-16:
(6*7)+(5*6)+(4*8)+(3*2)+(2*1)+(1*6)=118
118 % 10 = 8
So 7682-16-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H15NO3/c1-3-4-5-7(8(11)12)9-6(2)10/h7H,3-5H2,1-2H3,(H,9,10)(H,11,12)/t7-/m1/s1

7682-16-8 Well-known Company Product Price

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  • TCI America

  • (A0750)  N-Acetyl-DL-norleucine  >98.0%(T)

  • 7682-16-8

  • 1g

  • 190.00CNY

  • Detail
  • TCI America

  • (A0750)  N-Acetyl-DL-norleucine  >98.0%(T)

  • 7682-16-8

  • 25g

  • 990.00CNY

  • Detail

7682-16-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-acetamidohexanoic acid

1.2 Other means of identification

Product number -
Other names ACETYL-DL-2-AMINOHEXANOIC 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:7682-16-8 SDS

7682-16-8Relevant academic research and scientific papers

L-Methionine related 1-amino acids by acylase cleavage of their corresponding N-acetyl-DL-derivatives

Bommarius, Andreas S.,Drauz, Karlheinz,Guenther, Kurt,Knaup, Guenter,Schwarm, Michael

, p. 3197 - 3200 (2007/10/03)

Acylase I from Aspergillus oryzae is an even more useful enzyme than suggested so far. Besides standard amino acids such as L-Met, L-Val and L-Phe, a number of additional sulfur- and selenium-containing amino acids can be obtained at useful reaction rates and in very high enantiomeric purity by kinetic resolution of the respective N-acetyl-DL-amino acids.

NEW SYNTHESES OF α-AMINO ACIDS BASED ON N-ACYLIMINO ACETATES

Bretschneider, Thomas,Miltz, Wolfgang,Muenster, Peter,Steglich, Wolfgang

, p. 5403 - 5414 (2007/10/02)

The reaction of N-acylamino-2-bromoacetates 2 ( via N-acylimino acetates 3 ) with higher order mixed cuprates, trimethylsilyl enol ethers and β-dicarbonyl compounds leads to a variety of α-amino acid derivatives.Their conversion into the free amino acids can be conveniently carried out by the use of t-butyl protection.In case of the N-acetyl compounds cleavage of the protecting group and optical resolution can be achieved in one step hog renal acylase.

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