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GERANIOL, [1-3H] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

97068-23-0

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97068-23-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97068-23-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,0,6 and 8 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 97068-23:
(7*9)+(6*7)+(5*0)+(4*6)+(3*8)+(2*2)+(1*3)=160
160 % 10 = 0
So 97068-23-0 is a valid CAS Registry Number.

97068-23-0SDS

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 GERANIOL, [1-3H]

1.2 Other means of identification

Product number -
Other names -

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:97068-23-0 SDS

97068-23-0Downstream Products

97068-23-0Relevant articles and documents

INTERCONVERSION AND CYCLIZATION OF ACYCLIC ALLYLIC PYROPHOSPHATES IN THE BIOSYNTHESIS OF CYCLIC MONOTERPENOIDS IN HIGHER PLANTS

Suga, Takayuki,Hirata, Toshifumi,Aoki, Tadashi,Shishibori, Tsuyoshi

, p. 2769 - 2776 (2007/10/02)

Key Word Index - Biosynthesis; interconversion; cyclization; acyclic allylic pyrophosphates; cyclic monoterpenoids; higher plants.The biosynthesis of cyclic monoterpenoids has been investigated in both intact plants and cell-free extracts of several higher plants.The participation of a non-redox process in the biosynthesis of the cyclic monoterpenoids was indicated by the retention of all the tritium labels originating from mevalonic acid and geranyl, neryl and linalyl pyrophosphates.The cell-free extract catalysed the non-redox interconversions of geranyl, neryl and linalyl pyrophosphates to each other.By contrast, in both intact plants and cell-free extracts, the incorporation of linalyl pyrophosphate into the cyclic monoterpenoids occurred preferentially to the incorporation of neryl and geranyl pyrophosphates.These observations suggest the involvetment of a teriary allylic compound and/or its equivalent as a key intermediate, not only in the interconversion of the acyclic allylic pyrophosphates, but also in the formation of the cyclic monoterpenoids.

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