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82000-92-8

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82000-92-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82000-92-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,0,0 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 82000-92:
(7*8)+(6*2)+(5*0)+(4*0)+(3*0)+(2*9)+(1*2)=88
88 % 10 = 8
So 82000-92-8 is a valid CAS Registry Number.

82000-92-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methacryloyloxymethyl-5-nitrosalicylaldehyde

1.2 Other means of identification

Product number -
Other names 3-methacryloxymethyl-5-nitrosalicylaldehyde

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:82000-92-8 SDS

82000-92-8Relevant articles and documents

INDOLINOSPIROPYRANS WITH TWO POLYMERIZABLE GROUPS

Lyubimov, A. V.,Zaichenko, N. L.,Marevtsev, V. S.,Cherkashin, M. I.

, p. 585 - 587 (1982)

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Crystal and solution structures of photochromic spirobenzothiopyran. First full characterization of the meta-stable colored species

Hirano, Masafumi,Osakada, Kohtaro,Nohira, Hiroyuki,Miyashita, Akira

, p. 533 - 540 (2007/10/03)

Full elucidation for stable, colorless, and meta-stable colored structures of a new spirobenzothiopyran has been achieved both in the solid state and in a solution. 1′,3′,3′-Trimethyl-6-nitrospiro[(2H)-1-benzothiopyran-2, 2′-indoline] with an ester group as a substituent at the 8-position of 1-sp shows photochromism. The blue-green colored species resulted from UV irradiation (365 nm) in one minute and spontaneously bleaches within one minute in acetone and methanol at 27 °C. UV exposure (365 nm) of 1-sp in methanol for 3 h at room temperature results in the growth of deep blue needlelike single crystals of the open form of spirobenzothiopyran, photomerocyanine 1-pmc, whose structures in the solid state and in solution were obtained unambiguously. The X-ray structural analysis of 1-pmc revealed the molecular structure of the zwitterionic photomerocyanine with s-trans,s-trans conformation. 1-pmc is soluble to polar solvents and thermally returns to 1-sp. In the DMSO solution, 1-pmc is found to return slowly to 1-sp (1-pmc gave only 18% of 1-sp for 30 min at 22 °C). The detailed NMR studies in DMSO-d6 including COSY and NOE techniques as well as isotope labeling of the compound showed the structure with s-trans,s-cis conformation in a solution.

Synthesis and Photochemical Properties of Novel Spirobenzoselenazolinobenzopyrans

Hirano, Masafumi,Miyashita, Akira,Shitara, Hiroaki,Nohira, Hiroyuki

, p. 1873 - 1876 (2007/10/02)

5-Methoxy-3-methyl-6'-nitrospirobenzoselenazolinobenzopyrans have been newly prepared and their reversible structure changes induced by light were characterized by spectroscopic studies.Their stable colored-forms were identified as 5-methoxy-3-methylbenzoselenazolenium-2-trans-(5'-nitrostyryl-2'-oxide) being a zwitterionic structure.

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