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64318-28-1

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64318-28-1 Usage

Chemical Properties

White Solid

Uses

Intermediate in the preparation of Thyroxin derivatives.

Check Digit Verification of cas no

The CAS Registry Mumber 64318-28-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,3,1 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 64318-28:
(7*6)+(6*4)+(5*3)+(4*1)+(3*8)+(2*2)+(1*8)=121
121 % 10 = 1
So 64318-28-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H19NO3/c1-13(2,3)17-12(16)14-9-8-10-4-6-11(15)7-5-10/h4-7,15H,8-9H2,1-3H3,(H,14,16)

64318-28-1 Well-known Company Product Price

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  • Aldrich

  • (691550)  N-Boc-tyramine  97%

  • 64318-28-1

  • 691550-5G

  • 1,072.89CNY

  • Detail
  • Aldrich

  • (691550)  N-Boc-tyramine  97%

  • 64318-28-1

  • 691550-25G

  • 4,201.47CNY

  • Detail

64318-28-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-[2-(4-hydroxyphenyl)ethyl]carbamate

1.2 Other means of identification

Product number -
Other names N-Boc-2-(4-Hydroxyphenyl)ethylamine

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:64318-28-1 SDS

64318-28-1Relevant articles and documents

Tyramine fragment binding to BACE-1

Kuglstatter, Andreas,Stahl, Martin,Peters, Jens-Uwe,Huber, Walter,Stihle, Martine,Schlatter, Daniel,Benz, Joerg,Ruf, Armin,Roth, Doris,Enderle, Thilo,Hennig, Michael

, p. 1304 - 1307 (2008)

Fragment screening revealed that tyramine binds to the active site of the Alzheimer's disease drug target BACE-1. Hit expansion by selection of compounds from the Roche compound library identified tyramine derivatives with improved binding affinities as m

Investigation on the synthesis of new 3-[4-(Arylalkoxy)phenylethyl]-2-thioxo-1,3-thiazolidin-4-ones and their biological evaluation against cancer cells

Dago, Camille Déliko,N’ta Ambeu, Christelle,Coulibaly, Wacothon Karime,Békro, Yves-Alain,Mamyrbekova-Bekro, Janat A.,Le Guével, Rémy,Corlu, Anne,Bazureau, Jean-Pierre

, p. 341 - 349 (2017)

(Figure Presented) Herein, we report on the 5-step synthesis of new 3-[4-(arylalkoxy)phenylethyl]-2-thioxo-1,3-thiazolidin-4-ones without 5-arylidene fragments starting from tyramine The construction involved protection with Boc2O, regioselective O-alkyla

Chichibabin/isoChichibabin pyridinium synthesis of ma'edamines C and D

Hirose, Mika,Tanaka, Nao,Usuki, Toyonobu

supporting information, (2021/06/22)

Ma'edamines C and D were isolated from an Okinawan marine sponge and exhibited a unique tetrasubstituted pyridinium skeleton. The proposed biosynthetic pathway is similar to that of desmosine and isodesmosine, which are elastin-crosslinking amino acids. In this study, first total synthesis of ma'edamines C and D was achieved via Pr(OTf)3-promoted Chichibabin/isoChichibabin pyridinium synthesis starting from the corresponding aldehydes and amine.

COMPOSITION AND METHODS FOR TUMOR IMAGING AND TREATMENT

-

Paragraph 0125, (2021/11/13)

Radioisotope-labeled small molecule activity-based probes that target the cancer associated serine hydrolase neutral cholesterol ester hydrolase 1 (NCEH1) are described. The probes can undergo a reaction with the NCEH1, resulting in covalent bonding of a

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