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61676-63-9

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61676-63-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61676-63-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,6,7 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 61676-63:
(7*6)+(6*1)+(5*6)+(4*7)+(3*6)+(2*6)+(1*3)=139
139 % 10 = 9
So 61676-63-9 is a valid CAS Registry Number.

61676-63-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-propan-2-yloxy-1,3,2-benzodioxaborole

1.2 Other means of identification

Product number -
Other names Isopropyl-o-phenylenborat

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:61676-63-9 SDS

61676-63-9Relevant articles and documents

On titanium-promoted hydroborations of alkenes by borohydride and by catecholborane

Burgess, Kevin,Van Der Donk, Wilfred A.

, p. 3616 - 3620 (1994)

Some literature reports of catalyzed hydroborations of alkenes by the borohydride anion and by catecholborane were investigated to probe the actual mode of hydroboration. Reactions involving both TiCl3 and Ti(OiPr)4 seems to involve predominantly formation of BH3 in situ, although there is some evidence that the metal may be directly involved in a few cases. Ambiguity arises because it is shown that alkyl boronate esters can be formed by exchange between catecholborane and alkylboranes, so formation of these esters is not firm evidence of catalysis.

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