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1,3-Benzenedimethanethiol, 5-(1,1-dimethylethyl)-2-methoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77180-48-4

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77180-48-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77180-48-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,1,8 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 77180-48:
(7*7)+(6*7)+(5*1)+(4*8)+(3*0)+(2*4)+(1*8)=144
144 % 10 = 4
So 77180-48-4 is a valid CAS Registry Number.

77180-48-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [5-tert-butyl-2-methoxy-3-(sulfanylmethyl)phenyl]methanethiol

1.2 Other means of identification

Product number -
Other names -

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:77180-48-4 SDS

77180-48-4Relevant academic research and scientific papers

Synthesis and conformational studies of 9-methoxy- and 9-methyl- 2,11-dithia[3.3]metacyclophanes

Shimizu, Tomoe,Maeda, Takayuki,Hida, Katsuhiro,Yamato, Takehiko

scheme or table, p. 515 - 519 (2010/01/16)

A series of 9-methoxy- and 9-methyl-2,11-dithia[3.3]metacyclophanes are obtained by the coupling reaction of the corresponding 1,3-bis(bromomethyl) benzenes and bis(sulfanylmethyl)benzenes in ethanol under the high dilution conditions. The conformational

Synthesis of dibenzopyrenes and pyrenes via photolytic sulfur extrusion and intramolecular cross-coupling reactions of dithia[3.3] (1,3)naphthalenophanes and dithia[3.3]metacyclophanes

Ashram,Miller,Bridson,Georghiou

, p. 6476 - 6484 (2007/10/03)

The syntheses of several substituted dithia[3.3]metacyclophanes and dithia[3.3](1,3)naphthalenophanes are reported and their photolyses in triethyl or trimethyl phosphite are described. Under these conditions, the corresponding tetrahydrodibenzopyrenes and tetrahydropyrenes are produced in a one-pot procedure when the precursor dithianaphthalenophanes and dithiacyclophanes possess at least one intraannular methoxyl group. A mechanism with supporting evidence is proposed to account for these results. Structural determinations of the four isomeric 11,22-dimethoxy-2,13- dithia[3.3](1,3)naphthalenophanes by NMR and X-ray single-crystal diffraction studies are also described. The syntheses of the novel anti-transoid- and anti-cisoid-[2.2](1,3)naphthalenophanes are also described.

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