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36661-36-6

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36661-36-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36661-36-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,6,6 and 1 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 36661-36:
(7*3)+(6*6)+(5*6)+(4*6)+(3*1)+(2*3)+(1*6)=126
126 % 10 = 6
So 36661-36-6 is a valid CAS Registry Number.

36661-36-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-nitro-α-(2'-nitrophenyl)benzenemethanol

1.2 Other means of identification

Product number -
Other names Bis-(2-nitro-phenyl)-methanol

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:36661-36-6 SDS

36661-36-6Relevant articles and documents

Chemical synthesis of long RNAs with terminal 5′-phosphate groups

Pradère, Ugo,Halloy, Fran?ois,Hall, Jonathan

, p. 5210 - 5213 (2017)

Long structured RNAs are useful biochemical and biological tools. They are usually prepared enzymatically, but this precludes their site-specific modification with functional groups for chemical biology studies. One solution is to perform solid-phase synt

Photolabile protecting groups for nucleosides: Synthesis and photodeprotection rates

Hasan, Ahmad,Stengele, Klaus-Peter,Giegrich, Heiner,Cornwell, Paul,Isham, Kenneth R.,Sachleben, Richard A.,Pfleiderer, Wolfgang,Foote, Robert S.

, p. 4247 - 4264 (2007/10/03)

o-Nitrobenzyloxycarbonyl and a number of related groups have been tested for the photolabile protection of nucleoside 5'-hydroxyls. The rates of photodeprotection were found to vary by approximately 17-fold in a series of 5'-O-protected thymidine derivati

Photolysis of 2,2'-Dinitrodiphenylcarbinols in Neutral, Acidic and Basic Media

Jacob, E. Dominic,Joshua, C. P.

, p. 811 - 814 (2007/10/02)

Photolysis of various substituted 2,2'-dinitrodiphenylcarbinols (1a-c) has been carried out in 2-propanol, acidified ethanol and triethylamine. 2-Nitro-2'-nitrosobenzophenones (2a-c) are the major products.Small amounts of 3-(2'-nitrophenyl)-2,1-benzisoxa

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