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9003-49-0

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9003-49-0 Usage

Definition

ChEBI: A macromolecule composed of repeating butyl propionate units.

Check Digit Verification of cas no

The CAS Registry Mumber 9003-49-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 9,0,0 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 9003-49:
(6*9)+(5*0)+(4*0)+(3*3)+(2*4)+(1*9)=80
80 % 10 = 0
So 9003-49-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H12O2/c1-3-5-6-9-7(8)4-2/h4H,2-3,5-6H2,1H3

9003-49-0 Well-known Company Product Price

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  • Sigma-Aldrich

  • (181412)  Poly(butylacrylate)solution  25 wt. % in toluene, analytical standard, average Mw 60,000 (Typical), average Mn 20,000 (Typical)

  • 9003-49-0

  • 181412-10G

  • 1,437.93CNY

  • Detail
  • Aldrich

  • (181404)  Poly(butylacrylate)solution  average Mw ~99,000 by GPC, in toluene

  • 9003-49-0

  • 181404-50G

  • 1,959.75CNY

  • Detail

9003-49-0SDS

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 poly(butyl acrylate) macromolecule

1.2 Other means of identification

Product number -
Other names Butyl acrylate

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:9003-49-0 SDS

9003-49-0Relevant articles and documents

Acid- And base-switched palladium-catalyzed γ-C(sp3)-H alkylation and alkenylation of neopentylamine

Zhang, Jinquan,Zhang, Shuaizhong,Zou, Hongbin

supporting information, p. 3466 - 3471 (2021/05/31)

The functionalization of remote unactivated C(sp3)-H and the reaction selectivity are among the core pursuits for transition-metal catalytic system development. Herein, we report Pd-catalyzed γ-C(sp3)-H-selective alkylation and alkenylation with removable 7-azaindole as a directing group. Acid and base were found to be the decisive regulators for the selective alkylation and alkenylation, respectively, on the same single substrate under otherwise the same reaction conditions. Various acrylates were compatible for the formation of C(sp3)-C(sp3) and C(sp3)-C(sp2) bonds. The alkenylation protocol could be further extended to acrylates with natural product units and α,β-unsaturated ketones. The preliminary synthetic manipulation of the alkylation and alkenylation products demonstrates the potential of this strategy for structurally diverse aliphatic chain extension and functionalization. Mechanistic experimental studies showed that the acidic and basic catalytic transformations shared the same six-membered dimer palladacycle.

Synthesis of Some Aromatic and Aliphatic Esters Using WO3/ZrO2 Solid Acid Catalyst under Solvent Free Conditions

Guguloth, Vijaya Charan,Battu, Satyanarayana

, p. 2153 - 2157 (2020/09/16)

A simple method is delineated for the synthesis of substituted ester products in superior yields by esterification reaction under solvent unbound condition using tungsten upgraded ZrO2 solid acid catalyst at 353 K. The WO3/ZrO2 catalyst has been prepared by using impregnation method followed by calcination at 923 K over a period of 6 h in air atmosphere. SEM, XRD, FTIR, and BET surface area techniques were used to categorize this catalyst. Zirconia has both acidic and basic possessions which can be changed by incorporating suitable promoter atom like tungsten which in turn increases the surface area thereby enhancing the surface acidity. Impregnation of W6+ ions exhibits a strong influence on phase modification of zirconia from thermodynamically solid monoclinic to metastable tetragonal phase. Amalgamation of promoter W6+ will stabilize tetragonal phase which is active in catalyzing reactions. In esterification reaction WO3/ZrO2 catalyst was found to be stable, efficient and environmental friendly, effortlessly recovered by filtration, excellent yield of product and can be reusable efficiently.

Safe production process of butyl acrylate

-

Paragraph 0027-0046, (2020/07/15)

The invention relates to a safe production process of butyl acrylate, belonging to the technical field of organic synthesis. According to the invention, acrylic acid is used as an initial raw material; acrylate is prepared firstly; and then the acrylate reacts with bromobutane to synthesize the butyl acrylate. The safe production process has the following beneficial effects: (1) the use of acidicsubstances is avoided, and the corrosion of the acidic substances to pipelines is prevented; (2) reaction temperature is reduced; and (3) rectification separation effect is better, and the separated bromobutane can be repeatedly utilized.

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