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129848-88-0

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129848-88-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129848-88-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,8,4 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 129848-88:
(8*1)+(7*2)+(6*9)+(5*8)+(4*4)+(3*8)+(2*8)+(1*8)=180
180 % 10 = 0
So 129848-88-0 is a valid CAS Registry Number.

129848-88-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name BUTYRO-2,2-D2-PHENONE

1.2 Other means of identification

Product number -
Other names 1,3-benzodioxol-5-ylboronic acid pinacol ester

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:129848-88-0 SDS

129848-88-0Downstream Products

129848-88-0Relevant articles and documents

Dehydration-fragmentation mechanism of cathinones and their metabolites in ESI-CID

Matsuta, Shuntaro,Shima, Noriaki,Kakehashi, Hidenao,Ishikawa, Akari,Asai, Ryutaro,Nitta, Atsushi,Wada, Misato,Nakano, Shihoko,Kamata, Hiroe,Nishiyama, Yoshio,Nagatani, Hirohisa,Imura, Hisanori,Katagi, Munehiro

, (2020)

Various cathinone-derived designer drugs (CATs) have recently appeared on the drug market. This study examined the mechanism for the generation of dehydrated ions for CATs during electrospray ionization collision-induced dissociation (ESI-CID). The genera

Is the collosion induced loss of ethene from the (M - H+)- ion of butyrophenone a γ-hydrogen rearrangement?

Stringer, Michael B.,Underwood, Dennis J.,Bowie, John H.,Holmes, John L.,Mommers, Alexander A.,Szulejko, Jan E.

, p. 764 - 768 (2007/10/02)

The (M - H+)- ion of butyrophenone undergoes the following reactions on collisional activation: losses of CH3., CH4, (C,H5.), C2H4, C3H7., (CO + CH4), together with formation of C6H5- and C

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