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74076-63-4

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74076-63-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74076-63-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,0,7 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 74076-63:
(7*7)+(6*4)+(5*0)+(4*7)+(3*6)+(2*6)+(1*3)=134
134 % 10 = 4
So 74076-63-4 is a valid CAS Registry Number.

74076-63-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-methoxyphenyl)-4,7-dihydro-1,3-dioxepine

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:74076-63-4 SDS

74076-63-4Downstream Products

74076-63-4Relevant articles and documents

Lewis Acid-Catalyzed Vinyl Acetal Rearrangement of 4,5-Dihydro-1,3-dioxepines: Stereoselective Synthesis of cis- And trans-2,3-Disubstituted Tetrahydrofurans

Ghosh, Arun K.,Belcher, Miranda R.

, p. 10399 - 10412 (2020/09/02)

Lewis acid-catalyzed rearrangements of 4,5-dihydro-1,3-dioxepines have been investigated. Rearrangement of vinyl acetals under a variety of conditions resulted in cis- and trans-2,3-disubstituted tetrahydrofuran derivatives in a highly stereoselective man

Synthesis of the first photo-triggered pro-mitosene based on FR-900482

Williams, Robert M.,Rollins, Samuel B.,Judd, Ted C.

, p. 521 - 532 (2007/10/03)

A stereocontrolled synthesis of an eight-membered ring precursor to a photo-triggered mitosene is described. (C) 2000 Elsevier Science Ltd.

STEREOSPECIFIC SYNTHESIS OF A RIBOSYL-DIAZEPANONE DERIVATIVE; A SYNTHETIC APPROACH FOR ELUCIDATION OF THE STEREOCHEMISTRY OF A LIPID NUCLEOSIDE ANTIBIOTIC LIPOSIDOMYCIN B

Spada, Marianne R.,Ubukata, Makoto,Isono, Kiyoshi

, p. 1147 - 1167 (2007/10/02)

A new type of ribosyl-diazepanone derivative (23), the core ribosyl 7-membered heterocycle of the nucleoside antibiotic liposidomycin B has been synthesized using a chiral synthetic route that could offer accessibility to any of possible stereoisomers of

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