Welcome to LookChem.com Sign In|Join Free
  • or
1,4-Butanediol, 2,2-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

32812-23-0

Post Buying Request

32812-23-0 Suppliers

Recommended suppliers

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

32812-23-0 Usage

Physical state

Colorless, viscous liquid

Uses

a. Solvent
b. Industrial intermediate
c. Production of plastics and polymers
d. Synthesis of pharmaceuticals and other organic compounds

Derivation

Derived from butane

Flammability

Flammable

Health hazards

Vapor may cause drowsiness or dizziness if inhaled

Safety precautions

Handle with care and follow proper safety measures when working with it

Check Digit Verification of cas no

The CAS Registry Mumber 32812-23-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,8,1 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 32812-23:
(7*3)+(6*2)+(5*8)+(4*1)+(3*2)+(2*2)+(1*3)=90
90 % 10 = 0
So 32812-23-0 is a valid CAS Registry Number.

32812-23-0Relevant academic research and scientific papers

A phosphine-free iron complex-catalyzed synthesis of cycloalkanes: Via the borrowing hydrogen strategy

Bettoni, Léo,Gaillard, Sylvain,Renaud, Jean-Luc

supporting information, p. 12909 - 12912 (2020/11/07)

Herein we report a diaminocyclopentadienone iron tricarbonyl complex catalyzed synthesis of substituted cyclopentane, cyclohexane and cycloheptane compounds using the borrowing hydrogen strategy in the presence of various substituted primary and secondary 1,n diols as alkylating reagents. Deuterium labeling experiments confirm that the diols were the hydride source in this cascade process. This journal is

DERIVATIVES OF RELEBACTAM AND USES THEREOF

-

Paragraph 1429-1431, (2020/04/24)

Derivatives of relebactam, therapeutic methods of using the derivatives of relebactam, particularly in combination with β-lactam antibiotics and pharmaceutical compositions thereof are disclosed. The derivatives of relebactam are suitable for oral administration.

A Spiroalkylation Method for the Stereoselective Construction of α-Quaternary Carbons and Its Application to the Total Synthesis of (R)-Puraquinonic Acid

Elmehriki, Adam A. H.,Gleason, James L.

supporting information, p. 9729 - 9733 (2019/12/02)

Cyclic α-quaternary carbon stereocenters were prepared from biselectrophillic substrates and an easily prepared chiral bicyclic sulfonyl lactam. This was achieved in two steps by spiroalkylation, employing biphasic reaction conditions with a phase-transfer catalyst, followed by reduction and alkylation with a series of alkyl halide electrophiles. The products of this method were isolated in good yields with with high levels of diastereoselectivity. This methodology was employed in the enantioselective total synthesis of (R)-puraquinonic acid (1) for a late-stage installation of the α-quaternary carbon stereocenter. This enabled the shortest synthesis of 1 to date, an eight-pot sequence providing an overall yield of 14%.

AZTREONAM DERIVATIVES AND USES THEREOF

-

Paragraph 0990; 0991; 1150; 1151, (2019/04/18)

Disclosed herein are aztreonam derivatives, therapeutic methods of using the aztreonam derivatives, particularly in combination with β-lactamase inhibitors, and pharmaceutical compositions thereof. The aztreonam derivatives can be administered orally to provide orally bioavailable aztreonam.

Beta-lactamase inhibitors and uses thereof

-

Page/Page column 89, (2018/10/24)

β-Lactamase inhibiting compounds, therapeutic methods of using the β-lactamase inhibiting compounds, particularly in combination with β-lactam antibiotics and pharmaceutical compositions thereof are disclosed. The β-lactamase inhibiting compounds are suitable for oral administration.

A Palladium(II)-Catalyzed C-H Activation Cascade Sequence for Polyheterocycle Formation

Cooper, Stephen P.,Booker-Milburn, Kevin I.

supporting information, p. 6496 - 6500 (2015/06/02)

Polyheterocycles are found in many natural products and are useful moieties in functional materials and drug design. As part of a program towards the synthesis of Stemona alkaloids, a novel palladium(II)-catalyzed C-H activation strategy for the construction of such systems has been developed. Starting from simple 1,3-dienyl-substituted heterocycles, a large range of polycyclic systems containing pyrrole, indole, furan and thiophene moieties can be synthesized in a single step. Don't overdo it: A palladium(II)-catalyzed C-H activation cascade sequence for the synthesis of polyheterocycles is reported. Aromatization of the initially formed dihydro species occurred with a quinone oxidant. In some cases the use of one equivalent of the oxidant enabled isolation of the dihydro species as a single isomer (see scheme; X=NMe, O, S).

NOVEL COMPOUNDS FOR MODULATION OF ROR-GAMMA ACTIVITY

-

Paragraph 00450, (2014/03/22)

The present invention relates to aryl sulfones and related compounds that are modulators of ROR-gamma receptors. The invention also provides pharmaceutical compositions comprising these modulators, and methods of modulating ROR-gamma receptors using them. Also provided are methods of using aryl sulfones and related compounds as modulators of ROR-gamma to treat ROR-gamma mediated diseases

Total synthesis of ceratopicanol through tandem cycloaddition reaction of a linear substrate

Lee, Sang-Shin,Kim, Won-Yeob,Lee, Hee-Yoon

, p. 2450 - 2456,7 (2020/08/24)

Total synthesis of ceratopicanol (1) was achieved with a tandem cycloaddition reaction of allenyl diazo compound 6 via a trimethylenemethane (TMM) diyl intermediate. The TMM diyl mediated [2+3] cycloaddition reaction furnished the consecutive quaternary c

METHODS, COMPOUNDS, AND COMPOSITIONS FOR DELIVERING 1,3-PROPAN ED ISULFONIC ACID

-

Page/Page column 83, (2011/02/24)

The invention relates to methods, compounds, and compositions for delivering 1,3-propanedisulfonic acid (1,3PDS) in a subject, preferably a human subject. The invention encompasses compounds that will yield or generate 1,3PDS, either in vitro or in vivo. The invention also relates to sulfonate ester prodrugs of 1,3PDS as well as Gemini dimmers and oligomers of 1,3PDS for the prevention or treatment of associated diseases and conditions.

Lipase-catalyzed regioselective monoacetylation of unsymmetrical 1,5-primary diols

Oger, Camille,Marton, Zsuzsanna,Brinkmann, Yasmin,Burtel-Ponce, Valerie,Durand, Thierry,Graber, Marianne,Galano, Jean-Marie

supporting information; experimental part, p. 1892 - 1897 (2010/05/19)

"Chemical Equation Presented" Lipase B from Candida antarctica (CALB) has been selected as the most suitable enzyme to catalyze the regioselective monoacetylation of 1,5-diol isoprostane intermediate, using vinyl acetate as an acyl transfer reagent in TIIF. We next applied this reaction on linear 2-substituted, 2,2′-disubstituted-l,5pentanediols, and, cyclic 2,3-disubstituted-l,5-pentanediols. To rationalize the regioselectivity observed, molecular docking simulations were performed.

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 32812-23-0