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18804-91-6

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18804-91-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18804-91-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,8,0 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 18804-91:
(7*1)+(6*8)+(5*8)+(4*0)+(3*4)+(2*9)+(1*1)=126
126 % 10 = 6
So 18804-91-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H7NO3/c1-2-8-4(7)5-3-6/h3H,2H2,1H3,(H,5,6,7)

18804-91-6SDS

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 formyl-carbamic acid ethyl ester

1.2 Other means of identification

Product number -
Other names Formyl-urethan

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:18804-91-6 SDS

18804-91-6Relevant articles and documents

Extremely simple but long overlooked: Generation of α-Azido alcohols by hydroazidation of aldehydes

Banert, Klaus,Berndt, Christian,Firdous, Samia,Hagedorn, Manfred,Joo, Young-Hyuk,Rueffer, Tobias,Lang, Heinrich

supporting information; experimental part, p. 10206 - 10209 (2011/02/27)

Discovered by accident: Just because an example of a simple substructure cannot be found in literature does not mean that corresponding compounds are not readily accessible. α-Azido alcohols like 1-azidoethanol have now been prepared and isolated. Copyright

PHOTO-SENSITIZED OXYGENATION OF MONOCYCLIC 1H-1,3-DIAZEPINES

Kurita, Jyoji,Kojima, Hirokazu,Tsuchiya, Takashi

, p. 721 - 724 (2007/10/02)

The sensitized photooxygenation of monocyclic 1H-1,3-diazepines (1a-c) affords fragment products (2) to(7), which may be derived from the corresponding 4,7-endoperoxides (8) or the 4,5-dioxetanes (9) initially formed.The other possible dioxides and their decomposition products are not detected.

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