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65671-53-6

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65671-53-6 Usage

Uses

Boc-Lys(Me)2-OH is used in the synthesis of peptidyl α-keto thiazoles as tissue factor VIIa inhibitors. It is also used to prepare tetrahydropyranylglycine sulfonamides as bradykinin hB2 receptor antagonists.

Check Digit Verification of cas no

The CAS Registry Mumber 65671-53-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,6,7 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 65671-53:
(7*6)+(6*5)+(5*6)+(4*7)+(3*1)+(2*5)+(1*3)=146
146 % 10 = 6
So 65671-53-6 is a valid CAS Registry Number.

65671-53-6 Well-known Company Product Price

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  • Alfa Aesar

  • (H52437)  N(alpha)-Boc-N(epsilon),N(epsilon)-dimethyl-L-lysine, 97%   

  • 65671-53-6

  • 250mg

  • 882.0CNY

  • Detail
  • Alfa Aesar

  • (H52437)  N(alpha)-Boc-N(epsilon),N(epsilon)-dimethyl-L-lysine, 97%   

  • 65671-53-6

  • 1g

  • 2646.0CNY

  • Detail

65671-53-6SDS

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 (2S)-6-(dimethylamino)-2-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic acid

1.2 Other means of identification

Product number -
Other names N-[(tert-Butoxy)carbonyl]-N',N'-dimethyl-L-lysine

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:65671-53-6 SDS

65671-53-6Relevant articles and documents

ANTIBODY-CONJUGATED CHEMICAL INDUCERS OF DEGRADATION OF BRM AND METHODS THEREOF

-

Page/Page column 224, (2022/02/05)

The subject matter described herein is directed to antibody-CIDE conjugates (Ab-CIDEs) that target BRM for degradation, to pharmaceutical compositions containing them, and to their use in treating diseases and conditions where BRM degradation is beneficial.

Development of a fluorogenic probe with a transesterification switch for detection of histone deacetylase activity

Baba, Reisuke,Hori, Yuichiro,Mizukami, Shin,Kikuchi, Kazuya

supporting information, p. 14310 - 14313 (2012/11/07)

Histone deacetylases (HDACs) are key enzymatic regulators of many cellular processes such as gene expression, cell cycle, and tumorigenesis. These enzymes are attractive targets for drug development. However, very few simple methods for monitoring HDAC ac

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