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BOC-L-2-CYANOPHENYLALANINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

216312-53-7

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216312-53-7 Usage

Chemical Properties

White powder

Check Digit Verification of cas no

The CAS Registry Mumber 216312-53-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,6,3,1 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 216312-53:
(8*2)+(7*1)+(6*6)+(5*3)+(4*1)+(3*2)+(2*5)+(1*3)=97
97 % 10 = 7
So 216312-53-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H18N2O4/c1-15(2,3)21-14(20)17-12(13(18)19)8-10-6-4-5-7-11(10)9-16/h4-7,12H,8H2,1-3H3,(H,17,20)(H,18,19)/t12-/m1/s1

216312-53-7 Well-known Company Product Price

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  • Aldrich

  • (14984)  Boc-Phe(2-CN)-OH  ≥98.0% (TLC)

  • 216312-53-7

  • 14984-1G

  • 3,253.77CNY

  • Detail

216312-53-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Boc-2-cyano-L-phenylalanine

1.2 Other means of identification

Product number -
Other names (S)-2-tert-Butoxycarbonylamino-3-(2-cyano-phenyl)-propionic 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:216312-53-7 SDS

216312-53-7Relevant academic research and scientific papers

Lactam glycogen phosphorylase inhibitors and method of use

-

Page/Page column 39, (2010/02/05)

A compound of formula I wherein W is a bicyclic hetroaryl of the structure X is —O—, —S—, —SO2—, —CHR5—, —CHR5O—, —CHR5S—, —CHR5SO2—, —CHR5CO— or —CH2CHR5—;

A versatile synthesis of 2-substituted 4-amino-1,2,4,5-tetrahydro-2-benzazepine-3-ones

Van Rompaey, Karolien,Van Den Eynde, Isabelle,De Kimpe, Norbert,Tourwé, Dirk

, p. 4421 - 4432 (2007/10/03)

A mild and general strategy for the synthesis of 2-substituted 4-amino-1,2,4,5-tetrahydro-2-benzazepine-3-ones is described. The seven-membered lactam is prepared by intramolecular amide bond formation from the intermediate amino acid, which is obtained e

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