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105859-85-6

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105859-85-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105859-85-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,8,5 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 105859-85:
(8*1)+(7*0)+(6*5)+(5*8)+(4*5)+(3*9)+(2*8)+(1*5)=146
146 % 10 = 6
So 105859-85-6 is a valid CAS Registry Number.

105859-85-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N'-dimethyl-N,N'-hexamethylenebis(acetamide)

1.2 Other means of identification

Product number -
Other names N-[6-(Acetyl-methyl-amino)-hexyl]-N-methyl-acetamide

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:105859-85-6 SDS

105859-85-6Downstream Products

105859-85-6Relevant articles and documents

Lead optimization of HMBA to develop potent HEXIM1 inducers

Zhong, Bo,Lama, Rati,Ketchart, Wannarasmi,Montano, Monica M.,Su, Bin

, p. 1410 - 1413 (2014)

The potency of a series of Hexamethylene bis-acetamide (HMBA) derivatives inducing Hexamethylene bis-acetamide inducible protein 1 (HEXIM1) was determined in LNCaP prostate cancer cells. Several compounds with unsymmetrical structures showed significantly improved activity. Distinct from HMBA, these analogs have increased hydrophobicity and can improve the short half-life of HMBA, which is one of the factors that have limited the application of HMBA in clinics. The unsymmetrical scaffolds of the new analogs provide the basis for further lead optimization of the compounds using combinatorial chemistry strategy.

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