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843-55-0

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843-55-0 Usage

Chemical Properties

White Crystal

Check Digit Verification of cas no

The CAS Registry Mumber 843-55-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,4 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 843-55:
(5*8)+(4*4)+(3*3)+(2*5)+(1*5)=80
80 % 10 = 0
So 843-55-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H20O2/c19-16-8-4-14(5-9-16)18(12-2-1-3-13-18)15-6-10-17(20)11-7-15/h4-11,19-20H,1-3,12-13H2

843-55-0 Well-known Company Product Price

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  • Sigma-Aldrich

  • (77923)  Bisphenol?Z  analytical standard

  • 843-55-0

  • 77923-100MG

  • 458.64CNY

  • Detail
  • Aldrich

  • (450421)  4,4′-Cyclohexylidenebisphenol  98%

  • 843-55-0

  • 450421-25G

  • 512.46CNY

  • Detail

843-55-0SDS

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 1,1-Bis(4-Hydroxyphenyl)Cyclohexane

1.2 Other means of identification

Product number -
Other names 4-[1-(4-hydroxyphenyl)cyclohexyl]phenol

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:843-55-0 SDS

843-55-0Relevant articles and documents

Losev et al.

, p. 589 (1963)

Method for preparing high-purity kerley Bette

-

Paragraph 0033; 0034, (2016/10/07)

The invention relates to a preparation method of high-purity clinofibrate, the field of preparation of pharmaceutical compounds. The preparation method comprises the following steps: reacting cyclohexanone and phenol in concentrated hydrochloric acid and glacial acetic acid in a volume ratio of 3:1-7:1 to obtain an intermediate I crude product, decolorizing with a single solvent, and cooling to crystallize to obtain an intermediate I; reacting 2-methylbutyric acid with liquid bromine in phosphorus trichloride, reacting with anhydrous alcohol, extracting, and carrying out vacuum distillation to obtain an intermediate II; reacting the intermediate I and the intermediate II under solventless conditions to obtain an intermediate III; and hydrolyzing the intermediate III and sodium hydroxide, extracting, crystallizing to obtain a clinofibrate crude product; and recrystallizing with an anhydrous solvent to obtain the clinofibrate. The material proportion is adjusted to shorten the production operation period; the invention has the advantages of low energy consumption and low solvent consumption; and the obtained product has the advantages of uniform crystal grains, high purity and low cost.

Design of lamellar structured POSS/BPZ polybenzoxazine nanocomposites as a novel class of ultra low-k dielectric materials

Sasi Kumar,Ariraman,Alagar

, p. 19127 - 19136 (2014/05/20)

A novel class of lamellar structured polyhedral oligomeric silsesquioxane/bisphenol Z (POSS/BPZ) polybenzoxazine (PBz) nanocomposites was successfully designed by a facile one-step copolymerization technique. The chemical structures of the monomer and resulting polymer were characterized by Fourier transform infrared (FTIR) spectroscopy, 1H, 13C, DEPT-135, 29Si NMR (nuclear magnetic resonance) spectroscopy, X-ray diffraction (XRD), differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). The desired cross-linked lamellae structural arrangement of POSS/BPZ polybenzoxazine (PBz) nanocomposites was confirmed by transmission electron microscopy (TEM). The BPZ-PBz and POSS-PBz layers were self-assembled by intermolecular hydrogen bonding in such a way as to form the lamellar structure during ring opening polymerization. An advantage of this lamellar structure is that 30% POSS/BPZ polybenzoxazine composite exhibits an ultra low-k value of 1.7 at 1 MHz as well as high thermal stability. the Partner Organisations 2014.

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