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L-Cysteine, S-[2,3-bis[(1-oxohexadecyl)oxy]propyl]-N-(1-oxohexadecyl)-, 1,1-dimethylethyl ester, (R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87420-43-7

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87420-43-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87420-43-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,4,2 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 87420-43:
(7*8)+(6*7)+(5*4)+(4*2)+(3*0)+(2*4)+(1*3)=137
137 % 10 = 7
So 87420-43-7 is a valid CAS Registry Number.

87420-43-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name S-[2,3-bis(palmitoyloxy)-(2R)-propyl]-N-palmitoyl-(R)-cysteine tert-butyl ester

1.2 Other means of identification

Product number -
Other names Hexadecanoic acid (R)-2-((R)-2-tert-butoxycarbonyl-2-hexadecanoylamino-ethylsulfanyl)-1-hexadecanoyloxymethyl-ethyl ester

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:87420-43-7 SDS

87420-43-7Downstream Products

87420-43-7Relevant academic research and scientific papers

Stereochemical dependence of the self-assembly of the immunoadjuvants Pam3Cys and Pam3Cys-Ser

Reichel, Frank,Roelofsen, Annie M.,Geurts, Hubertus P. M.,Haemaelaeinen, Taina I.,Feiters, Martinus C.,Boons, Geert-Jan

, p. 7989 - 7997 (1999)

The lipopeptide tripalmitoyl-S-glycerylcysteme (Pam3Cys) is derived from the N-terminal part of bacterial lipopeptides and is a polyclonal B-lymphocyte and macrophage activator. Derivatives of Pam3Cys constitute highly potent, nontoxic immunoadjuvants, and lipopeptide - antigen conjugates have found important applications as novel fully synthetic low-molecular-weight vaccines. To establish a possible correlation between molecular structure, aggregation properties, and biological activities, we have studied the self-assembly and monolayer properties of a range of Pam3Cys derivatives using transmission electron microscopy (TEM) and a Langmuir-film balance combined with a Brewster angle microscopy (BAM). It was found that the chirality of the glyceryl moiety and the additional serine unit impacted on the mode of aggregation and the monolayer properties. Correlations are discussed between these physicochemical properties and biological activities.

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