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7-iodohept-1-ene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

107175-49-5

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107175-49-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107175-49-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,1,7 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 107175-49:
(8*1)+(7*0)+(6*7)+(5*1)+(4*7)+(3*5)+(2*4)+(1*9)=115
115 % 10 = 5
So 107175-49-5 is a valid CAS Registry Number.

107175-49-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-hepten-1-yl iodide

1.2 Other means of identification

Product number -
Other names .7-iodo-1-heptene

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:107175-49-5 SDS

107175-49-5Upstream product

107175-49-5Relevant academic research and scientific papers

Novel potent apoA-I peptide mimetics that stimulate cholesterol efflux and pre-β particle formation in vitro

Ingenito, Raffaele,Burton, Charlotte,Langella, Annunziata,Chen, Xun,Zytko, Karolina,Pessi, Antonello,Wang, Jun,Bianchi, Elisabetta

, p. 236 - 239 (2010)

Reverse cholesterol transport (RCT) is believed to be the primary mechanism by which HDL and its major protein apoA-I protect against atherosclerosis. Starting from the inactive 22-amino acid peptide representing the consensus sequence of the class A amphipathic helical repeats of apoA-I, we designed novel peptides able to mobilize cholesterol from macrophages in vitro, and to stimulate the formation of 'nascent HDL' particles, with potency comparable to the entire apoA-I protein.

INTRAMOLEKULARE CYCLOADDITIONEN MIT ISOBENZOFURANEN - III. EIN HYDRIERTES NAPHTHOTHIOPHEN AUS EINEM 1-ALKENYLTHIENOFURAN

Schoening, A.,Friedrichsen, W.

, p. 1137 - 1138 (2007/10/02)

The synthesis of tetrahydronaphthothiophene 6 utilizing an intramolecular Diels-Alder reaction with an 1-alkenylthienofuran 4 is described.

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