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87357-67-3

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87357-67-3 Usage

Chemical Properties

Light Yellow Liquid

Check Digit Verification of cas no

The CAS Registry Mumber 87357-67-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,3,5 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 87357-67:
(7*8)+(6*7)+(5*3)+(4*5)+(3*7)+(2*6)+(1*7)=173
173 % 10 = 3
So 87357-67-3 is a valid CAS Registry Number.
InChI:InChI=1/C21H34O3/c1-2-3-4-5-6-7-8-9-13-16-20(17-21(22)23)24-18-19-14-11-10-12-15-19/h10-12,14-15,20H,2-9,13,16-18H2,1H3,(H,22,23)/t20-/m1/s1

87357-67-3SDS

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 (3R)-3-phenylmethoxytetradecanoic acid

1.2 Other means of identification

Product number -
Other names (3R)-3-(phenylmethoxy)-tetradecanoic acid

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:87357-67-3 SDS

87357-67-3Downstream Products

87357-67-3Relevant articles and documents

BIFUNCTIONAL COMPOUND AND ITS USE IN IMMUNOTHERAPY

-

, (2021/02/12)

The invention relates to a bifunctional compound that is, on one side, an agonist of the TLR4 and, on the other side, an important inhibitor of the PSMA. Said compound is useful in immunotherapy for the treatment and/or prevention of prostate cancer. Therefore, the invention also relates to the use of the compound and to the pharmaceutical composition comprising it.

SYNTHETIC DERIVATIVES OF MPL AND USES THEREOF

-

, (2014/11/13)

In one aspect, the present disclosure provides compounds of formulae (I) and (II). In another aspect, a compound of formula (I) or (II) is formulated into compositions with an antigen, optionally with a vesicle. In some embodiments, compositions are administered intramuscularly.

Preparation of a lipid A derivative that contains a 27-hydroxyoctacosanoic acid moiety

Santhanam, Balaji,Boons, Geert-Jan

, p. 3333 - 3336 (2007/10/03)

(Chemical Equation Presented) A general synthetic strategy for long-chain ω-1 hydroxy fatty acids has been developed, which employs as a key reaction step a cross metathesis between ω-unsaturated ester and 3-butene-2-ol. The resulting lipids were used for

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