Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1732-09-8

Post Buying Request

1732-09-8 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1732-09-8 Usage

Chemical Properties

clear colorless to slightly yellow liquid

Uses

Dimethyl suberate was used in the preparation of [8-2H2] and [7-2H2]oleates.

Check Digit Verification of cas no

The CAS Registry Mumber 1732-09-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,3 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1732-09:
(6*1)+(5*7)+(4*3)+(3*2)+(2*0)+(1*9)=68
68 % 10 = 8
So 1732-09-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O4/c1-13-9(11)7-5-3-4-6-8-10(12)14-2/h3-8H2,1-2H3

1732-09-8 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (B22681)  Dimethyl suberate, 99%   

  • 1732-09-8

  • 25g

  • 516.0CNY

  • Detail
  • Alfa Aesar

  • (B22681)  Dimethyl suberate, 99%   

  • 1732-09-8

  • 100g

  • 1698.0CNY

  • Detail

1732-09-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Dimethyl suberate

1.2 Other means of identification

Product number -
Other names Octanedioic acid dimethyl ester

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:1732-09-8 SDS

1732-09-8Relevant articles and documents

-

Morgan,Walton

, p. 290,291 (1935)

-

Absolute stereochemistry of petroformynes, high molecular polyacetylenes from the marine sponge Petrosia ficiformis

Guo, Yuewei,Gavagnin, Margherita,Trivellone, Enrico,Cimino, Guido

, p. 13261 - 13268 (1994)

The absolute stereochemistry of some petroformynes (1-7), characteristic metabolites of the Mediterranean sponge Petrosia ficiformis displaying terminal 1-yn-3-ol-4-ene moieties, has been elucidated by applying high field 1H-NMR to Mosher method. Esterification of Petrosia polyacetylenes with (R)- and (S)-α-methoxy-α-trifluoromethylphenylacetyl (MTPA) chloride yielded the corresponding (S)- and (R)-MTPA esters. Careful NMR measurements led to assign the S absolute stereochemistry at all the chiral centers of petroformynes. The R absolute stereochemistry of 3-hydroxydocosa-4(E) 15(E)-dien-1-yne (8), previously established on the basis of a questionable extention of the application of the exciton chirality method, is confirmed by applying advanced Mosher method. The structures of petroformyne-5 (7) and petroformyne-8 (11) are now supported by additional evidence.

TARGET PROTEIN EED DEGRADATION-INDUCING DEGRADUCER, PREPARATION METHOD THEREOF, AND PHARMACEUTICAL COMPOSITION FOR PREVENTING OR TREATING DISEASES RELATED TO EED, EZH2, OR PRC2, COMPRISING SAME AS ACTIVE INGREDIENT

-

, (2021/12/23)

The present invention relates to a target protein degradation-inducing Degraducer, a preparation method thereof, and a pharmaceutical composition for preventing or treating diseases related to EED, EZH2, or PRC2 comprising same as an active ingredient. A novel compound represented by formula 1, according to the present invention is a Degraducer compound that induces degradation of a target protein, i.e., embryonic ectoderm development (EED) or polycomb repressive complex 2 (PRC2), utilizing cereblon E3 ubiquitin ligase, von Hippel-Lindau tumor suppressor (VHL) E3 ubiquitin ligase, mouse double minute 2 homolog (MDM2) E3 ubiquitin ligase, and cellular inhibitor of apoptosis protein 1 (cIAP) E3 ubiquitin ligase, wherein the compound has an aspect of remarkably achieving target protein degradation-inducing activity through a ubiquitin proteasome system (UPS), and therefore there is a useful effect in that it is possible to provide a pharmaceutical composition for preventing or treating diseases or conditions related to a target protein, and a functional health food composition for preventing or improving same, comprising said compound as an active ingredient.

Ultralow-Molecular-Weight Stimuli-Responsive and Multifunctional Supramolecular Gels Based on Monomers and Trimers of Hydrazides

Wu, Dehua,Song, Jintong,Qu, Lang,Zhou, Weilan,Wang, Lei,Zhou, Xiangge,Xiang, Haifeng

supporting information, p. 3370 - 3378 (2020/10/02)

The simpler, the better. A series of simple, neutral and ultralow-molecular-weight (MW: 140–200) hydrazide-derived supramolecular gelators have been designed and synthesized in two straightforward steps. For non-conjugated cyclohexane-derived hydrazides, their monomers can self-assemble to form gels through intermolecular hydrogen bonds and dipole-dipole interactions. Significantly, conjugated phthalhydrazide can self-aggregate into planar and circular trimers through intermolecular hydrogen bonds and then self-assemble to form gels through intermolecular π–π stacking interactions. It is interesting that these simple gelators exhibit unusual properties, such as self-healing, multi-response fluorescence, and visual and selective recognition of chiral (R)/(S)-1,1′-binaphthalene-2,2′-diamine and S2? through much different times of gel re-formation and blue-green color change, respectively. These results underline the importance of supramolecular gels and extend the scope of supramolecular gelators.

Methylation of mono- and dicarboxylic acids with dimethyl carbonate catalyzed with binder-free zeolite NaY

Khusnutdinov,Shchadneva,Mayakova, Yu. Yu.,Konovalova, Yu. S.,Khazipova,Kutepov

, p. 163 - 168 (2017/04/24)

Synthesis of methyl mono- and dicarboxylates was developed consisting in treating the corresponding acids with dimethyl carbonate in the presence of a heterogenic catalyst, crystalline aluminosilicate whose mechanically strong granules to 90–95% were built of crystal aggregates of zeolite Y with modulus of about 5.0 in the Na-form. Optimum catalyst and reagents ratio and the reaction conditions were found for the preparation in high yields of methyl esters of mono- and dicarboxylic acids.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 1732-09-8