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(5S)-3-[(8R,11R)-8,11-dihydroxy-11-{(2R,5R)-5-[(1R)-1-hydroxypentadecyl]tetrahydrofuran-2-yl}undecyl]-5-methylfuran-2(5H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

177534-99-5

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177534-99-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 177534-99-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,5,3 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 177534-99:
(8*1)+(7*7)+(6*7)+(5*5)+(4*3)+(3*4)+(2*9)+(1*9)=175
175 % 10 = 5
So 177534-99-5 is a valid CAS Registry Number.

177534-99-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-4-[(8R,11R)-8,11-dihydroxy-11-[(2R,5R)-5-[(1R)-1-hydroxypentadecyl]oxolan-2-yl]undecyl]-2-methyl-2H-furan-5-one

1.2 Other means of identification

Product number -
Other names 2(5H)-Furanone,3-((8R,11R)-8,11-dihydroxy-11-((2R,5R)-tetrahydro-5-((1R)-1-hydroxypentadecyl)-2-furanyl)undecyl)-5-methyl-,(5S)

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:177534-99-5 SDS

177534-99-5Upstream product

177534-99-5Downstream Products

177534-99-5Relevant academic research and scientific papers

Total synthesis of the threo, trans, threo-mono-tetrahydrofuran annonaceous acetogenin longifolicin

Marshall, James A.,Jiang, Hongjian

, p. 1493 - 1496 (1998)

An enantioselective synthesis of the C35 threo, trans, threo-mono-tetrahydrofuran annonaceous acetogenin longifolicin through use of chiral long-chain α-and γ-OMOM allylic stannanes and (E)-ethyl 3-formyl-2-propenoate as the starting materials

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