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176590-77-5

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176590-77-5 Usage

General Description

(2R,3R)-2,3-Dihydroxybutane-1,4-diyl dibenzoate is a chemical compound with the molecular formula C20H20O6. It is a diester of 2,3-dihydroxybutane-1,4-diol and benzoic acid, and it consists of two hydroxybutane units linked by an ester bond. (2R,3R)-2,3-DIHYDROXYBUTANE-1,4-DIYL DIBENZOATE is commonly used as a crosslinking agent in the production of polymers and resins, as well as a stabilizer in plastics and rubber. It is also used as an intermediate in the synthesis of various organic compounds. The diester structure of (2R,3R)-2,3-dihydroxybutane-1,4-diyl dibenzoate makes it a versatile and valuable chemical in the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 176590-77-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,5,9 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 176590-77:
(8*1)+(7*7)+(6*6)+(5*5)+(4*9)+(3*0)+(2*7)+(1*7)=175
175 % 10 = 5
So 176590-77-5 is a valid CAS Registry Number.
InChI:InChI=1/C18H18O6/c19-15(11-23-17(21)13-7-3-1-4-8-13)16(20)12-24-18(22)14-9-5-2-6-10-14/h1-10,15-16,19-20H,11-12H2/t15-,16-/m1/s1

176590-77-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2R,3R)-4-benzoyloxy-2,3-dihydroxybutyl] benzoate

1.2 Other means of identification

Product number -
Other names (2R,3R)-2,3-Dihydroxybutane-1,4-diyl dibenzoate

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:176590-77-5 SDS

176590-77-5Relevant articles and documents

CYCLIC COMPOUND

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Paragraph 0302, (2018/04/13)

The present invention provides compounds having a Toll-like receptor 4 (TLR4) signaling inhibitory action useful as preventive and therapeutic drugs of autoimmune disease and/or inflammatory disease or diseases such as chemotherapy-induced peripheral neuropathy (CIPN), chemotherapy-induced neuropathic pain (CINP), liver injury, ischemia-reperfusion injury (IRI) and the like. The present invention relates to a compound represented by formula (I) and a salt thereof: (wherein, each symbol is explained in greater detail in the specification).

CYCLIC COMPOUNDS

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Paragraph 0704; 0705; 0706, (2016/11/24)

The present invention provides compounds having a Toll-like receptor 4 (TLR4) signaling inhibitory action useful as preventive and therapeutic drugs of inflammatory disease and/or central nervous system disease or diseases such as chemotherapy-induced peripheral neuropathy (CIPN), chemotherapy-induced neuropathic pain (CINP), liver injury, ischemia-reperfusion injury (IRI) and the like. The present invention relates to a compound represented by formula (I) and a salt thereof: (wherein, each symbol is explained in greater detail in the specification).

Synthesis of spiro C-arylglycoriboside via Pd(II)-catalyzed spirocyclization

Awasaguchi, Ken-Ichiro,Miyazawa, Masahiro,Uoya, Ikuyo,Inoue, Koichi,Nakamura, Koji,Yokoyama, Hajime,Kakuda, Hiroko,Hirai, Yoshiro

experimental part, p. 2392 - 2396 (2010/12/18)

Spiro C-arylglycoriboside was synthesized in 21 steps via Pd(II)-catalyzed spirocyclization as a key reaction. Hemiketal was obtained in 47% overall yield from cis-2-butene-1,4-diol and spirocyclized with PdCl2(PhCN) 2 in dilute THF solution (0.01 M) to afford the 1,6-dioxaspiro[4.4] nonane skeleton in high yield. The spirocyclo adduct was transformed into spiro C-arylglycoriboside in five steps. Georg Thieme Verlag Stuttgart New York.

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