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14949-49-6

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14949-49-6 Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 34, p. 207, 1969 DOI: 10.1021/jo00838a045

Check Digit Verification of cas no

The CAS Registry Mumber 14949-49-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,9,4 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 14949-49:
(7*1)+(6*4)+(5*9)+(4*4)+(3*9)+(2*4)+(1*9)=136
136 % 10 = 6
So 14949-49-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H10O/c1-2-7-10-9(5-1)6-3-4-8-11-10/h1-3,5-7H,4,8H2

14949-49-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dihydro-1-benzoxepine

1.2 Other means of identification

Product number -
Other names 2,3-dihydro-1-benzoxepin

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:14949-49-6 SDS

14949-49-6Relevant articles and documents

Titanocene(II)-promoted cyclization of unsaturated thioacetals

Fujiwara, Tooru,Takeda, Takeshi

, p. 354 - 356 (1999)

The low-valent titanium species-promoted transformation of unsaturated thioacetals to cyclic compounds was studied. The cyclization of thioacetals having an olefin moiety proceeded with the loss of terminal olefin carbon to produce the corresponding five-

Role of the gem-difluoro moiety in the tandem ring-closing metathesis-olefin isomerization: Regioselective preparation of unsaturated lactams

Fustero, Santos,Sanchez-Rosello, Maria,Jimenez, Diego,Sanz-Cervera, Juan F.,Del Pozo, Carlos,Acena, Jose Luis

, p. 2706 - 2714 (2007/10/03)

Careful selection of the metathesis catalyst, solvent, and reaction conditions allows for the efficient and regioselective synthesis of isomeric fluorinated and nonfluorinated lactam derivatives II and III from precursor amides I through a ring-closing me

2,3,4,5-tetrahydro-1-benzoxepins, the use thereof and pharmaceutical products based on these compounds

-

, (2008/06/13)

2,3,4,5-Tetrahydro-1-benzoxepins of the formula I STR1 with R1 equaling, inter alia, H, alkyl, alkoxy, Hal, alkylsulfonyl, arylsulfonyl, R2 equaling H, alkyl, alkoxy, OH, R3 to R6 H or alkyl and X equaling STR2 have excellent efficacy as antihypertensives, as coronary therapeutics, as agents for the treatment of cardiac insufficiency, of disturbances of cerebral and peripheral blood flow or of disturbances of intestinal motility, premature labor, obstructions of the airways or of the urinary tract or of the biliary tract or as spasmolytics.

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