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N-BOC-1-PIVALOYL-D-ERYTHRO-SPHINGOSINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

342649-71-2

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342649-71-2 Usage

Chemical Properties

White Solid

Check Digit Verification of cas no

The CAS Registry Mumber 342649-71-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,2,6,4 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 342649-71:
(8*3)+(7*4)+(6*2)+(5*6)+(4*4)+(3*9)+(2*7)+(1*1)=152
152 % 10 = 2
So 342649-71-2 is a valid CAS Registry Number.
InChI:InChI=1/C28H53NO5/c1-8-9-10-11-12-13-14-15-16-17-18-19-20-21-24(30)23(22-33-25(31)27(2,3)4)29-26(32)34-28(5,6)7/h20-21,23-24,30H,8-19,22H2,1-7H3,(H,29,32)/b21-20+/t23-,24+/m1/s1

342649-71-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,3R,E)-2-((tert-butoxycarbonyl)amino)-3-hydroxyoctadec-4-en-1-yl pivalate

1.2 Other means of identification

Product number -
Other names -

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:342649-71-2 SDS

342649-71-2Downstream Products

342649-71-2Relevant academic research and scientific papers

Sphingomyelin analogues as inhibitors of sphingomyelinase

Taguchi, Minoru,Sugimoto, Kikuo,Goda, Ken-Ichi,Akama, Tomoko,Yamamoto, Kyoko,Suzuki, Taizo,Tomishima, Yasumitsu,Nishiguchi, Mariko,Arai, Koshi,Takahashi, Kenzo,Kobori, Takeo

, p. 1963 - 1966 (2003)

To search for neutral sphingomyelinase inhibitors we designed and synthesized hydrolytically stable analogues of sphingomyelin. The novel compounds 8 and 9 which were replaced the phosphodiester moiety of sphingomyelin with the carbamate moiety showed inhibitory activity with an IC50 value of μM on neutral sphingomyelinase in rat brain microsomes. Compound 8i showed a selective neutral sphingomyelinase inhibitory activity.

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